|
VAERS ID: |
2362796 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Wisconsin |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Product administered to patient of inappropriate age, Product administration error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Client received Pfizer COVID-19 vaccine for 5-11 yr olds. Client is only 4 years old. Parent was informed at the time the error occurred. |
|
VAERS ID: |
2362807 (history) |
Form: |
Version 2.0 |
Age: |
0.75 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Vit D and EPIPEN JR prescribed Current Illness: Tested for food allergies Preexisting Conditions: None Allergies: NKA Diagnostic Lab Data: None CDC Split Type: Write-up: Patient was given a dose of 0.2 ml out of a vial that had not been diluted |
|
VAERS ID: |
2362981 (history) |
Form: |
Version 2.0 |
Age: |
0.5 |
Sex: |
Male |
Location: |
Maryland |
Vaccinated: |
2022-06-29 |
Onset: |
2022-06-30 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
A5141413 / 1 |
LL / - |
Administered by: Private Purchased by: ? Symptoms: Brief resolved unexplained event, Cardiac monitoring normal, Electrocardiogram normal, Unresponsive to stimuli SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Neonatal disorders (broad), Hypotonic-hyporesponsive episode (broad), Respiratory failure (narrow), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? Yes, 1 days Extended hospital stay? No Previous Vaccinations: Other Medications: Vitamin d Current Illness: 2-3 weeks prior he had a slight runny nose. Negative rapid tests (took tests over the course of three days - the entire family). Dad took a negative PCR. Preexisting Conditions: None. Allergies: None Diagnostic Lab Data: EKG 6/30 - Normal O2 sat and HR monitor overnight with admission 6/30-7/1. Normal overnight. CDC Split Type: Write-up: 24 hours post-vaccine baby had a BRUE. While changing his diaper he went unresponsive and I questioned if he was breathing. I startled him back with shouting his name. He then became unresponsive again. This occurred 4-5 times over 1-2 minutes. I attempted startling and tryingg go to get a reaction and he became alert again. I took him to the ER where he was diagnosed as having a BRUE and was kept on monitors overnight. |
|
VAERS ID: |
2362991 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-06-23 |
Onset: |
2022-07-01 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
A514163 / 1 |
LA / SYR |
Administered by: Other Purchased by: ? Symptoms: Induration, Injection site erythema, Injection site reaction, Injection site swelling, Pain in extremity, Skin exfoliation, Skin warm SMQs:, Severe cutaneous adverse reactions (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Hiya Multivitamin; Nova Ferrum Liquid Iron Supplement Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: vsafe Write-up: He said his arm was hurting. I took off his shirt to look and it was warm to the touch. It was really red, swollen, and hard. I put come ice on it and called the doctor. He said it felt better after we applied the ice and he took a nap like normal. once we talked to the doctor, it got redder that day. It was very bright beet red. The hole where the injection was now visible. It was super red around it. Before it was flat, then it was swollen and visible. The doctor told me to outline it to track if it was infected or not. It did spread outside of that line, but the redness went down as I was icing it. She told me to give him Benadryl at night before bed to see if that helped then Zyrtec during the day. She said to call back if it did not become better. In the morning, I called again because it spread outside of the original line. The first day it was really red and bright looking. The next day it was bigger but lighter and less angry looking. The nurse told me to give him some Zyrtec and to keep icing and watching it. She saw the pictures and said it did look better. She said to call back again if it doesn''t continue getting better. IT?s gotten better each day and there is a faint spot where it was. It?s faintly red and the skin is peeling a little bit around the injection site. |
|
VAERS ID: |
2362996 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-06-03 |
Onset: |
2022-06-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Incorrect dose administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: no tests needed no adverse events seen CDC Split Type: Write-up: the patient took the Pfizer dose of pediatrics instead of the toddler dose but the mother gave the incorrect date of birth of the patient. The patient''s actual age was 4 at the time of the vaccine administration of their first Pfizer dose. The patient was notified that the wrong dose was given to them, but they were aware that they gave the incorrect date of birth of the child. This was discovered on 7/7/22 when the father returned for the child''s second dose. |
|
VAERS ID: |
2363118 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
New Jersey |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-08 |
Days after vaccination: |
7 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Fatigue, Hypersomnia, Hypophagia, Influenza A virus test negative, Influenza B virus test, Pyrexia, SARS-CoV-2 test negative, Streptococcus test negative SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Depression (excl suicide and self injury) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Multivitamin with flouride Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: 07/08/22 -Streptococcus group A RNA: Negative -Influenza virus A + B + SAR-Cov-2 (COVID 19) Ag panel, rapid IA, upper respiratory specimen: Negative CDC Split Type: Write-up: Patient developed a 102.1 fever at around 6:30 am on 07/08/2022. She was tired throughout the day, slept more than she typically does, and did not eat much at meals. |
|
VAERS ID: |
2363142 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Male |
Location: |
Montana |
Vaccinated: |
2022-07-06 |
Onset: |
2022-07-08 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 1 |
LL / SYR |
Administered by: Private Purchased by: ? Symptoms: Decreased appetite, Fatigue, Irritability, Pain, Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Fever, fatigue, loss of appetite, fussy, in pain-achy |
|
VAERS ID: |
2363144 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Washington |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-01 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Circumstance or information capable of leading to medication error, Product administered to patient of inappropriate age, Wrong product administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: NONE Allergies: NONE Diagnostic Lab Data: NONE CDC Split Type: Write-up: When I was drawing up 4 year vaccine . The Assistant of that doctor in which i was helping with vaccine, told me to do COVID VACCINE to another Room Also. I misheard and understood they were 7 years old. I drew up 5-11 PFIZER vaccine instead of 6month- 4 years MODERNA vaccine and administered to 4 year old patient. |
|
VAERS ID: |
2363145 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Washington |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-01 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: NONE Allergies: NONE Diagnostic Lab Data: NONE CDC Split Type: Write-up: When I was drawing up 4 year vaccine . The Assistant of that doctor in which i was helping with vaccine, told me to do COVID VACCINE to another Room Also. I misheard and understood they were 7 years old. I drew up 5-11 PFIZER vaccine instead of 6month- 4 years MODERNA vaccine and administered to 4 year old patient. |
|
VAERS ID: |
2363147 (history) |
Form: |
Version 2.0 |
Age: |
1.75 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Work Purchased by: ? Symptoms: Blood glucose normal, Cardiac monitoring, Crying, Decreased appetite, Eye movement disorder, Fatigue, Muscle rigidity, Pyrexia, Skin discolouration SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (narrow), Depression (excl suicide and self injury) (broad), Ocular motility disorders (narrow), Hypotonic-hyporesponsive episode (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None. Covid 5 weeks ago Preexisting Conditions: None Allergies: None Diagnostic Lab Data: EMS measured blood pressure, temperature, blood sugar, and put some leads on his body to monitor his heart. ED measured temperature, O2 level, and heart rate. CDC Split Type: Write-up: Woke up after nap very tired. Cried getting diaper changed. Refused snack/drink. Started to fall, eyes rolled back, skin tone looked gray/blue, body went rigid for about 2 minutes. EMS arrived within 10 min. HR at 180 bpm. Febrile 102F. Blood sugar 112 mg/dL |
|
VAERS ID: |
2363150 (history) |
Form: |
Version 2.0 |
Age: |
1.58 |
Sex: |
Female |
Location: |
Arizona |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-08 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
017B22A / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Incorrect dosage of mRNA COVID-19 vaccine product was inadvertently administered. Patient received Moderna 100 ?g 0.5 ml age not indicated |
|
VAERS ID: |
2363858 (history) |
Form: |
Version 2.0 |
Age: |
1.08 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2022-06-23 |
Onset: |
2022-06-23 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-09 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / - |
Administered by: Private Purchased by: ? Symptoms: Body temperature, Product administered at inappropriate site, Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug abuse and dependence (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient''s Medical History (including any illness at time of vaccination): None Allergies: Diagnostic Lab Data: Test Date: 20220701; Test Name: fever; Result Unstructured Data: Test Result:gone down; Comments: almost 105 degrees to 102 degrees CDC Split Type: USPFIZER INC202200920318 Write-up: prolonged high fever; Anatomical Location of Administration of Pfizer vaccine considered as suspect: Left Thigh; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from medical information team. The reporter is the parent. A 13-month-old female patient received BNT162b2 (BNT162B2), on 23Jun2022 at 11:45 as dose 1, single (Lot number: FT9142) at the age of 13 months, in left thigh for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: mmr, administration date: 05May2022, when the patient was 12-month-old, for Immunisation, reaction(s): "Diarrhea". The following information was reported: PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 23Jun2022 at 11:45, outcome "unknown", described as "Anatomical Location of Administration of Pfizer vaccine considered as suspect: Left Thigh"; PYREXIA (medically significant) with onset 25Jun2022, outcome "not recovered", described as "prolonged high fever". The event "prolonged high fever" required emergency room visit. The patient underwent the following laboratory tests and procedures: Body temperature: (01Jul2022) gone down, notes: almost 105 degrees to 102 degrees. The patient did not receive any other vaccines within four weeks prior to the vaccination. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available)was none reported.; Sender''s Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal association between the events and suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate. |
|
VAERS ID: |
2363947 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Missouri |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-09 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LL / IM |
Administered by: Public Purchased by: ? Symptoms: Chills, Diarrhoea, Pain SMQs:, Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: She developed pain, diarrhea, chills, and temperature of 100.4 |
|
VAERS ID: |
2363969 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Pennsylvania |
Vaccinated: |
2022-07-09 |
Onset: |
2022-07-09 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-09 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Blood glucose, Cold sweat, Cough, Heart rate decreased, Hypotonia, Pallor SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Citirizine Multi vit Current Illness: none Preexisting Conditions: none Allergies: Animal Dander Peanut Sesame Seed Diagnostic Lab Data: BP''s/P/Glucose CDC Split Type: Write-up: Child waiting with dad after vaccination. After 15min, father states that child coughed and started calling out and slowing falling over. No loss of consciousness. Father alerted staff. They were brought to a patient room. Doctort was alerted and was in the room with child. Child very pale. Skin cool and clammy. Decreased heart rate to 59 and blood pressure was 72/38. Glucose was 89. Blood pressure retaken after 5 min. (72/36) Pulse was 72. Color slowly returned to his face. Cool water and cookies given. Child eating and drinking. Father states, "He looks much better." Episode lasted approximately 15 min. |
|
VAERS ID: |
2364019 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-09 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-09 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
- / SYR |
Administered by: Private Purchased by: ? Symptoms: Peripheral swelling, Rash erythematous, Vaccination site rash, Vaccination site reaction SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None needed CDC Split Type: Write-up: Large red rash around vaccination site 8 days after vaccine was given. Also a little swollen. |
|
VAERS ID: |
2364131 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Nebraska |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-03 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-10 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 1 |
- / - |
Administered by: Unknown Purchased by: ? Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None known Current Illness: None known Preexisting Conditions: History of tetralogy of fallot s/p repair Allergies: None known Diagnostic Lab Data: N/A CDC Split Type: Write-up: Whole body rash occuring 48-72 hours after vaccination. |
|
VAERS ID: |
2364146 (history) |
Form: |
Version 2.0 |
Age: |
1.33 |
Sex: |
Female |
Location: |
New Jersey |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-10 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LL / IM |
Administered by: Other Purchased by: ? Symptoms: Diarrhoea, Vomiting SMQs:, Acute pancreatitis (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Flu like symptoms for roughly 3 days after receiving MMR vaccine at 13 months Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Nine Diagnostic Lab Data: Went to Hospital ER on 7/9 in the evening. Was prescribed zofran on 7/9. Has been frequently drinking Pedialyte. CDC Split Type: Write-up: Received first moderna shot at 4:30pm on 7/8. Diarrhea and vomiting began at 7:30pm on 7/8. Continued diarrhea and vomiting on 7/9 and 7/10. |
|
VAERS ID: |
2364158 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Rhode Island |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-08 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-10 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
RA / SYR |
Administered by: Private Purchased by: ? Symptoms: Rash, Rash pruritic, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: n/a Current Illness: June 13, 2022 one day of isolated cough and congestion, rapid covid negative. Preexisting Conditions: n/a Allergies: n/a Diagnostic Lab Data: N/A. CDC Split Type: Write-up: Picked up from school 7/8 between 1730-1800. Noted to have hives most prominent on abdomen, right face, right arm, left arm. Rash was pruritic. Improved with diphenhydramine. Continued to wax and wane for 48 hours (time of report). Rash primarily located bilateral cheeks, abdomen, bilateral arms. No other symptoms. No known new exposure at school or detergents. |
|
VAERS ID: |
2364321 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Ohio |
Vaccinated: |
2022-06-24 |
Onset: |
2022-06-24 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Patient was given the wrong dose of vaccine- was given the Pfizer vaccine for 5-11 years of age |
|
Vaccinated: |
2022-07-06 |
Onset: |
2022-07-06 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/a Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None done to date CDC Split Type: Write-up: Patient was given the inappropriate dose of 1.25 ml of Moderna instead of 0.25ml. This was discovered after the patient had left but the provider called the mother to discuss the adverse event. Provider and Mom had thorough discussion and to this point the patient has not any reaction to the immunization dosage of 1.25 ml. Mom was advised to report any side effects the child has. |
|
VAERS ID: |
2364360 (history) |
Form: |
Version 2.0 |
Age: |
1.67 |
Sex: |
Female |
Location: |
Wisconsin |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-01 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
- / IM |
Administered by: Private Purchased by: ? Symptoms: Product administration error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: CDC Split Type: Write-up: Vaccine was reconstituted on the previous day and beyond the recommended 12 hour mark. Phone call made to Pfizer who supplied studies supporting vaccine continues to be stable up to 24 hours after reconstituting. Patient was vaccinated just shy of the 24 hour mark. Patient did not have any adverse effects, this was an administration error. |
|
VAERS ID: |
2364364 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Wisconsin |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-01 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
- / IM |
Administered by: Private Purchased by: ? Symptoms: Product administration error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: Vaccine was reconstituted on the previous day and beyond the recommended 12 hour mark. Phone call made to Pfizer who supplied studies supporting vaccine continues to be stable up to 24 hours after reconstituting. Child was vaccinated just shy of the 24 hour mark. Child did not have any adverse effects, this was an administration error. |
|
VAERS ID: |
2364369 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Oregon |
Vaccinated: |
2022-06-30 |
Onset: |
2022-07-08 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Erythema, Swelling, Tenderness SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Flonase Current Illness: Diagnosis of campylobacter about a month earlier Preexisting Conditions: Seasonal allergies Allergies: Seasonal allergies (no specific testing) Diagnostic Lab Data: N/A CDC Split Type: Write-up: Large local area of erythema (5 x 3.5 cm) and swelling noted on 7/8 (8 days after initial injection) with mild tenderness but no fever or other symptoms. Initially worsened but started topical triamcinolone and has been gradually improving but not yet fully resolved. |
|
VAERS ID: |
2364406 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Connecticut |
Vaccinated: |
2022-06-25 |
Onset: |
2022-07-02 |
Days after vaccination: |
7 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
- / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Peripheral swelling, Rash, Vaccination site erythema, Vaccination site mass SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: Multivitamins Current Illness: No Preexisting Conditions: No Allergies: No Diagnostic Lab Data: No CDC Split Type: vsafe Write-up: On July 2, 2022 we noticed a small red bump at the vaccine site. On July 3, 2022 we noticed the red bump had gotten bigger and her arm was swollen and also had a rash, the swelling went down some but we took her to a walk-in clinic as it was a Sunday. The doctors at the clinic said it looked like what they were seeing as a delayed reaction to the Moderna vaccine. Give it until Wednesday to see if it would subside some or go away all together. By Wednesday it was completely gone. |
|
VAERS ID: |
2364525 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Washington |
Vaccinated: |
2022-06-24 |
Onset: |
2022-07-02 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: Gait disturbance, Pain in extremity SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Upper respiratory infection a week before the vaccination (Non COVID-19 related) Preexisting Conditions: None Allergies: Tree Nuts Diagnostic Lab Data: None CDC Split Type: vsafe Write-up: It started that Saturday the week after the vaccine. He woke up and said his leg started hurting and didn?t want to walk on it. When he did walk on it, he was limping. Later in the day, he started walking on it and was eventually just fine. Several days passed, and he reported the same symptoms another day when he woke up. There was leg pain, and he didn?t want to walk on it. The 2nd day was July 6, 2022 and continued on into the 7th. Since it persisted, we decided to make a doctor?s appointment which is later today. He?s still complaining of leg pain and there?s still a limp, but not as bad as it was. I didn?t notice any redness or swelling as well. |
|
VAERS ID: |
2364585 (history) |
Form: |
Version 2.0 |
Age: |
1.17 |
Sex: |
Male |
Location: |
Virginia |
Vaccinated: |
2022-06-22 |
Onset: |
2022-07-04 |
Days after vaccination: |
12 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LG / IM |
Administered by: Public Purchased by: ? Symptoms: COVID-19, Cough, Ear infection, Rhinorrhoea, SARS-CoV-2 test negative, SARS-CoV-2 test positive SMQs:, Anaphylactic reaction (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: Two rapid test (positive) and two PCR test (negative). CDC Split Type: vsafe Write-up: After the vaccine, he was fine. He had a runny nose and a cough around July 2. On July 4 and July 6 he tested positive with the rapid test but tested negative on the PCR test on the same day. We had the PCR test done at the local ER. The ER doctor stated he had an ear infection and that our rapid test was wrong. They provided us with a prescription for amoxicillin. He is feeling better but he still has a runny nose. |
|
VAERS ID: |
2364607 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
2022-07-02 |
Onset: |
2022-07-10 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Injection site induration, Injection site rash, Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: daily multi-vitamin gummy gummy fiber supplement Current Illness: n/a Preexisting Conditions: does get nose bleeds Allergies: n/a Diagnostic Lab Data: CDC Split Type: Write-up: A rash around the injection site with a hard bump underneath. He said it didn''t itch or hurt. Showed up a week after the injection. Looks to be getting better after day two of rash. |
|
VAERS ID: |
2364647 (history) |
Form: |
Version 2.0 |
Age: |
1.33 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-11 |
Onset: |
2022-07-11 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FP7150 / 1 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: No Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type: Write-up: 16 month old arrives to clinic with mother for vaccine update, however patient was administered 12 and older (gray cap) Pfizer ( COVID 19) by error. After realizing my administration error supervisor was notified immediately. Patient''s PCP, medical director, director of immunization department and patient''s mother where notified of error/incident. VEARS report was created, mother wrote an incident report, mother of patient was advised by PCP if patient develops any adverse reactions to please head to the emergency room. In case patient has any questions or concerns mother was advised to contact the clinic. Supervisor will be following up with patient. |
|
VAERS ID: |
2364666 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
North Carolina |
Vaccinated: |
2022-06-30 |
Onset: |
2022-07-01 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Excessive eye blinking SMQs:, Ocular motility disorders (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: No known food or drug allergies Diagnostic Lab Data: None CDC Split Type: Write-up: Patient''s parents reported noticing frequent eye blinking while watching tv the day after receiving her COVID19 vaccine and continuing intermittently. She has no eye irritation/ pain, does not seem to be aware she is doing this. no prior eye injury. She did not exhibit this behavior prior to her COVID19 vaccine. Patient was not evaluated for this concern- her dad reported it to me during her younger brother''s well visit on 7/5/22. |
|
VAERS ID: |
2364728 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-11 |
Onset: |
2022-07-11 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR9237B / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Rash erythematous SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: NONE Allergies: NONE Diagnostic Lab Data: N/A CDC Split Type: Write-up: WITHIN 5 MIN AFTER RECEIVING PEDIATRIC COVID-19 MODERNA VACCINE, PATIENT DEVELOPED SEVERAL RASH-LIKE RED SPOTS ON BOTH LOWER ARMS, BUT NOT AT THE INJECTION SITE. PATIENT SAID HIS BREATHING WAS FINE, AND NO ITCHINESS WHERE THE SPOTS WERE. MOM WAS ADVISED TO GIVE PATIENT BENADRYL WHEN GET HOME. I SPOKE TO MOM ON THE PHONE AROUND 4PM--SHE SAID HER DAD GAVE PATIENT 2.5ML BENADRYL AND PATIENT IS DOING FINE. |
|
VAERS ID: |
2365965 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Massachusetts |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-08 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-11 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Unknown Current Illness: No Preexisting Conditions: No Allergies: No Diagnostic Lab Data: N/A CDC Split Type: Write-up: Urticaria noted on trunk less than 24 hours after vaccine resolved with use of Benadryl. |
|
VAERS ID: |
2365837 (history) |
Form: |
Version 2.0 |
Age: |
0.5 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-07 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / UNK |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Off label use SMQs: Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: 6 month old was given a 0.25 ml (50 mcg) dose out of the red cap vial; This spontaneous case was reported by an other health care professional and describes the occurrence of OFF LABEL USE (6 month old was given a 0.25 ml (50 mcg) dose out of the red cap vial) in a 6-month-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On 07-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 07-Jul-2022, the patient experienced OFF LABEL USE (6 month old was given a 0.25 ml (50 mcg) dose out of the red cap vial). At the time of the report, OFF LABEL USE (6 month old was given a 0.25 ml (50 mcg) dose out of the red cap vial) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant information was reported. It was reported that no signs of adverse events were noted after administration. No treatment information was provided. |
|
VAERS ID: |
2365866 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
New Mexico |
Vaccinated: |
2022-07-06 |
Onset: |
2022-07-06 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FP7135 / 1 |
- / - |
Administered by: Public Purchased by: ? Symptoms: Product use issue, Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Medication errors (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USPFIZER INC202200936356 Write-up: rash around the shoulder area spread a little ways down towards belly and down the back; lot number FP7135; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). A 2-year-old female patient received BNT162b2 (BNT162B2), on 06Jul2022 at 14:30 as dose 1, single (Lot number: FP7135) at the age of 2 years, in left leg for covid-19 immunisation. The patient''s relevant medical history was not reported. There were no concomitant medications. The following information was reported: PRODUCT USE ISSUE (non-serious) with onset 06Jul2022 at 13:30, outcome "unknown", described as "lot number FP7135"; RASH (non-serious) with onset 06Jul2022 at 13:45, outcome "recovering", described as "rash around the shoulder area spread a little ways down towards belly and down the back". The events "rash around the shoulder area spread a little ways down towards belly and down the back" required emergency room visit. Therapeutic measures were taken as a result of rash. Additional information: No other vaccine received in four weeks and no other medications in two weeks. Patient was not received covid prior vaccination and not tested covid post vaccination. It was reported that patient had a rash that wasn''t a severe reaction couple of mins after the shot. Was around the shoulder area and under the neck both front and back and rash spread a little ways down towards belly and down the back. AE resulted in Emergency room/department or urgent care. Doctor checked and gave Benadryl. No follow-up attempts are possible. No further information is expected. |
|
VAERS ID: |
2365975 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Kansas |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LL / IM |
Administered by: Public Purchased by: ? Symptoms: No adverse event, Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: n/a Current Illness: n/a Preexisting Conditions: n/a Allergies: n/a Diagnostic Lab Data: n/a CDC Split Type: Write-up: The Moderna 6mo-5Years was diluted with 2.2ml of 0.9% sodium chloride (normal saline, preservative -free diluent. Administered .2ml to left vastus lateralis. Parent notified 07/08/22 at 4:55pm of incident. No adverse reaction at that time. Educated parent to signs and symptoms of adverse reactions. A follow up call will ensue with the CDC recommendations for further vaccination information. |
|
VAERS ID: |
2365977 (history) |
Form: |
Version 2.0 |
Age: |
1.42 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2022-07-11 |
Onset: |
2022-07-11 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / SYR |
Administered by: Private Purchased by: ? Symptoms: Body temperature increased, Febrile convulsion, Feeling abnormal, Lethargy, Loss of consciousness, Seizure, Skin warm, Unresponsive to stimuli, Viral test negative SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Convulsions (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? Yes Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: Virology panel was all negative. CDC Split Type: Write-up: After receiving vaccination, patient was out of it for approximately ~15 mins, after that period seemed lethargic but otherwise normal. Patient showed no other adverse reaction until time for his nap at 12:40p, when he felt warm to the touch but underarm temperature reading was 98.7. He woke up atypically early at 2:50p, but laid in crib seemingly playing quietly. At 3:56p, mother heard whimpering sound and went to check on patient who was convulsing and unconscious until EMS arrived at 4:03p, he was very hot but EMS was unable to get an accurate temperature reading. Convulsions stopped when paramedics arrived at approx. 4:03p and patient was unresponsive for an additional approx. 10 mins. Patient was placed under ice by EMS and had a temperature reading of 102.4 when he arrived Hospital in approx 20-30 mins later. |
|
VAERS ID: |
2365998 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Kansas |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LL / IM |
Administered by: Public Purchased by: ? Symptoms: No adverse event, Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: n/a Current Illness: n/a Preexisting Conditions: n/a Allergies: n/a Diagnostic Lab Data: n/a CDC Split Type: Write-up: The Moderna 6mo-5Years was diluted with 2.2ml of 0.9% sodium chloride (normal saline, preservative -free diluent. Administered .2ml to left vastus lateralis. Parent notified 07/08/22 at 4:49pm of incident. No adverse reaction at that time. Educated parent to signs and symptoms of adverse reactions. A follow up call will ensue with the CDC recommendations for further vaccination information. |
|
VAERS ID: |
2366036 (history) |
Form: |
Version 2.0 |
Age: |
1.08 |
Sex: |
Female |
Location: |
Tennessee |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, Product preparation error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: n/a Current Illness: n/a Preexisting Conditions: n/a Allergies: n/a Diagnostic Lab Data: N/a. CDC Split Type: Write-up: A 13month old was inadvertently given a higher than recommended dose of 3mcg for 6month to < 5years. The nurse did not dilute the vial at all and drew up 0.2mL of vaccine and administered it to patient. We realized the mistake within the 15min that the patient was here waiting. We reached out to VAERS, Pfizer Medical information, and ED on what we needed to next for patient. Dr. went into and told the mom that she received a higher than recommended dose. She discussed possible side effects and signs and symptoms to look out for. Gave her her personal number and advised to go directly to ED or call 911 if any symptoms develop. |
|
VAERS ID: |
2366040 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Colorado |
Vaccinated: |
2022-07-09 |
Onset: |
2022-07-09 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (NOVAVAX)) / NOVAVAX |
FL8094 / 1 |
- / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: at around noon I was doing end of day covid vaccine count to discard unused doses, and I noticed my count for 5-11 doses was off I should have been wasting 6 but there was only 5, I should of also had 10 9 waste of the tender age Pfizer covid but had all 10, this patient''s mother had asked to receive Pfizer and Pfizer was ordered upon check in since I did the patients vitals. MA who administered. when I looked at the 5-11 covid admin sheet, this patients sticker was on. I then realized this patient has received a 5-11 covid Pfizer vax instead of the appropriately ordered Pfizer tender aged vax.I checked MAR to see if MA had scanned vax or manually entered. vaccine had been manually entered and therefore no hard stop would have been noticed by MA administering. Dose is counted and does not need to be repeated |
|
VAERS ID: |
2366178 (history) |
Form: |
Version 2.0 |
Age: |
1.67 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-09 |
Onset: |
2022-07-11 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Herpes zoster, Varicella virus test positive SMQs:, Opportunistic infections (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: Varicella zoster culture positive. CDC Split Type: Write-up: Shingles/varicella Zoster infection to right leg. |
|
VAERS ID: |
2366189 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Puerto Rico |
Vaccinated: |
2022-07-04 |
Onset: |
2022-07-05 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
AR / SYR |
Administered by: Public Purchased by: ? Symptoms: Diarrhoea, Fatigue, Laboratory test normal, Loss of personal independence in daily activities, SARS-CoV-2 test negative, Viral infection, Vomiting SMQs:, Acute pancreatitis (broad), Dementia (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: COVID-19 test: negative. CDC Split Type: vsafe Write-up: Day of the vaccine she started to become fatigued. The next day at night she started to vomit. No noticeable pain or discomfort other than continuous vomiting. She went to school the next day however she did come home early. At day 3 post vaccine she started to have diarrhea as well. On Friday she started to feel better however continued to have diarrhea. On Saturday she was feeling back to normal. Went to a swimming class and in the late afternoon she began to vomit again and have diarrhea as well. We took her to ER and they did all the tests including COVID-19 tests and all were negative. They believe that it was due to a viral infection. The doctors did not believe it was due to the vaccine. She had IV fluids and was sent home. She has started feeling much better as of Saturday. |
|
VAERS ID: |
2366237 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Maryland |
Vaccinated: |
2022-07-05 |
Onset: |
2022-07-06 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LL / IM |
Administered by: Other Purchased by: ? Symptoms: Diet refusal, Lethargy, Malaise, Pyrexia, SARS-CoV-2 test negative, Streptococcus test negative SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: COVID-19 test - negative; Strep test - negative. CDC Split Type: vsafe Write-up: The night of the vaccine, she developed a fever and woke up. She has had a fever ever since the vaccine. She is lethargic and will not eat. I took her to the urgent care on 7/8/2022. She had a strep and COVID-19 test that were negative. Her highest fever was 104. I also took her to the ER yesterday. She is currently still sick. |
|
VAERS ID: |
2366268 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR9237B / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Lip swelling, Swelling face, Swelling of eyelid, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Periorbital and eyelid disorders (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Eczema and tree nut allergy Allergies: Tree Nut Allergy Diagnostic Lab Data: CDC Split Type: Write-up: Dose 1 given at 11:01 and at about 11:16 AM father alerted us that his son was rubbing his face and scratching his neck. Face swollen with swelling of bilateral eyelids, upper lip swollen and visible hives on face and neck. Mouth was OK and no wheezes heard. Benadryl was offered at 11:25 and after about 10-15min the swelling of the eyelids and lip subsided and most of the facial hives gone and only a few remaining hives on neck. Observed until 11:45 and given instructions on when to return. Also, family has epipens at home for the preexisting tree nut allergy |
|
VAERS ID: |
2366384 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2022-07-10 |
Onset: |
2022-07-10 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LL / SYR |
Administered by: Other Purchased by: ? Symptoms: Fatigue, Injection site pain, Poor quality sleep, Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Depression (excl suicide and self injury) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: Covid more than 10 days before vaccination Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type: Write-up: Patient developed a fever the evening of the 10th (the day he was vaccinated) and continued to have a fever for the entire following day. It was difficult to take his temperature but at one point, it was 101.5 even after he had take Tylenol. He also experienced pain at his injection site. He slept very poorly the evening of the 10th and was very tired the following day. By the morning of the 12th he appeared to be recovered, though he was still experiencing some tenderness at the injection site, as evidenced by him being afraid to put pants on because he didn''t want anyone to touch his thigh. |
|
VAERS ID: |
2366408 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Washington |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-07 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Public Purchased by: ? Symptoms: Injection site extravasation, Vaccination error SMQs:, Extravasation events (injections, infusions and implants) (narrow), Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: unknown Current Illness: unknown Preexisting Conditions: unknown Allergies: unknown Diagnostic Lab Data: unknown CDC Split Type: Write-up: Patient was present in the clinic on 7/7/2022 for her 1st dose of Pfizer (6 months ? 4yrs formulation, lot number FT9142). RN, the vaccinator, went ahead to vaccinated on the right vastus lateralis, however when the needle (25G vanishing point) was 1/4 of the way piercing into the child skin; the child moved. The vaccinator attempted to follow and continue to insert the needle. Upon injecting, the dose was leaking at the injection site. Vaccinator and parent were able to witness that almost none of the dose enter the site. RN was able to assess the site for any scratching or bruising as well assessed for any bleeding. RN notified the Charge nurse, who was able to educate parent on the need for repeating dose on different site (left vastus lateralis) per our protocol, since less than half ? or rather none of the dose had entered the site. The parent was educated on watching the child for any bruising and that the child can be given children?s Tylenol for comfort. Parent expressed understanding and consented to re-administration of dose in opposite site. Client was able to successfully receive dose. |
|
VAERS ID: |
2366475 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-06 |
Onset: |
2022-07-06 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Unknown Purchased by: ? Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: RASH |
|
VAERS ID: |
2366562 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Alaska |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Unknown Current Illness: None. Preexisting Conditions: None. Allergies: NKA Diagnostic Lab Data: None CDC Split Type: Write-up: Pizer Pediatric vaccine 5-11 yr old formulation given to a 4 year old child in error. |
|
VAERS ID: |
2366563 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Georgia |
Vaccinated: |
2022-06-22 |
Onset: |
2022-06-29 |
Days after vaccination: |
7 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LA / SYR |
Administered by: Public Purchased by: ? Symptoms: Immunisation reaction, Injection site erythema, Injection site pain, Injection site pruritus, Injection site rash, Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Unilateral Hearing Loss / Profound Hearing Loss at her left ear. Normal Hearing at her right ear. No other health conditions. Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: *No serious adverse reactions - patient remained healthy. Exactly one week after receiving first COVID vaccine shot (Moderna) - patient (3yr) developed redness / slightly swollen marks at the injection site. The rash grew quickly to form one large area around the injection site. She commented early during onset that the area was itchy and tender, but it wasn''t painful. The large, slightly swollen, red rash remained for about 24 hours and then began to dissipate and slowly loose redness until completely going away. Based on comparison images online - it seems to match "covid arm" or "modern arm" similar to the reactions had by other adult modern vaccine recipients. |
|
VAERS ID: |
2366567 (history) |
Form: |
Version 2.0 |
Age: |
1.5 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
2022-07-06 |
Onset: |
2022-07-07 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-12 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 1 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Cough, Decreased appetite, Fatigue, Pyrexia SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Cough, treatment: prednisolone Fatigue Fever, treatment: acetaminophen Loss of appetite |
|
VAERS ID: |
2367327 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Florida |
Vaccinated: |
2022-07-09 |
Onset: |
2022-07-09 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 1 |
LL / IM |
Administered by: Other Purchased by: ? Symptoms: Wrong product administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Error: Wrong Age for Vaccine Given- |
|
VAERS ID: |
2367393 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2022-06-27 |
Onset: |
2022-07-05 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Injection site erythema, Injection site rash SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Redness/rash at injection site when he woke up on day 8 post shot. |
|
VAERS ID: |
2367497 (history) |
Form: |
Version 2.0 |
Age: |
0.5 |
Sex: |
Female |
Location: |
Indiana |
Vaccinated: |
2022-07-05 |
Onset: |
2022-07-08 |
Days after vaccination: |
3 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9147 / 1 |
LL / - |
Administered by: Public Purchased by: ? Symptoms: Cough, Pyrexia, Respiratory tract congestion, SARS-CoV-2 test negative SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Fever after getting one of her general pediatric shots. However it was only for a day and then symptoms would go away. Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: Over Counter Rapid Test: Negative CDC Split Type: vsafe Write-up: Friday, 2 days after the vaccine, daycare called us around 03:00PM and indicated that she had a fever over 101. We called the pediatrician and they instructed us to give her acetaminophen for symptoms. Since Friday, she has been experiencing waves of on and off fevers as well. She started to have a slight cough and congestion however no runny nose. Over the counter COVID-19 test showed negative result. Pediatrician examined and did not find anything in ears, nose, throat, or lungs. They did not see anything concerning however some respiratory symptoms. |
|
VAERS ID: |
2367534 (history) |
Form: |
Version 2.0 |
Age: |
0.58 |
Sex: |
Female |
Location: |
Virginia |
Vaccinated: |
2022-06-29 |
Onset: |
2022-07-03 |
Days after vaccination: |
4 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / SYR |
Administered by: Public Purchased by: ? Symptoms: Eye infection, Eye swelling, Full blood count abnormal, Neutropenia, Neutrophil count decreased SMQs:, Anaphylactic reaction (broad), Agranulocytosis (broad), Angioedema (narrow), Haematopoietic leukopenia (narrow), Ocular infections (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? Yes, 4 days Extended hospital stay? No Previous Vaccinations: Other Medications: poly vi sol Current Illness: none Preexisting Conditions: Prematurity (33w 4d) Allergies: none Diagnostic Lab Data: CBC (7/3-7/7) CDC Split Type: Write-up: Eye infection, neutropenia. Eye swelling began 7/3, admitted 7/4, CBC showed low (<100) neutrophil. Antibiotics administered, discharged 7/7 |
|
VAERS ID: |
2367611 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2022-07-09 |
Onset: |
2022-07-10 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / SYR |
Administered by: Public Purchased by: ? Symptoms: Fatigue, Pyrexia, SARS-CoV-2 test negative, Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Topical Cream for Eczema Current Illness: N/A Preexisting Conditions: N/A Allergies: Peanuts; Cashews Diagnostic Lab Data: COVID-19 Test: Negative CDC Split Type: vsafe Write-up: We started to notice that after lunch she vomited out her entire lunch while driving over to a friends house. After that, she seemed fine and played in the pool for a bit and everything was normal she did sleep over an hour and a half and seemed a little more tired than usual. After getting home later that evening we noticed that she began to run a small fever. We did not give her anything for the symptoms and she seemed to be fine and slept the entire night through. We then took her to the pediatrician the next day she still had a fever of 100, and at the visit they measured a temperature at 101. COVID-19 test was done and came back negative, they said she was well hydrated, everything else looked great. After getting home she took a two hour nap. Tylenol was given in the middle of the afternoon and fever went down and she seemed completely fine. As of the 12th, she has been completely fine and non symptomatic. |
|
VAERS ID: |
2367710 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Virginia |
Vaccinated: |
2022-06-30 |
Onset: |
2022-07-02 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: Eye swelling, Hordeolum SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Ocular infections (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: vitamins-multi, C, iron, probiotic, etc Current Illness: fever of 101 and vomiting one week prior. incident resolved itself over a period of 7 hours. Preexisting Conditions: Preemie twin born at 30 weeks. Gross motor skill delays and sensory integration issues. Allergies: none knoen Diagnostic Lab Data: CDC Split Type: Write-up: stye in left eye. then a week later, major swelling in right eye. both new occurrences with no history before vaccine |
|
VAERS ID: |
2367720 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Extra dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: No medications. No known dietary supplements or herbal remedies known at time at vaccination Current Illness: No known illnesses at time of vaccination and up to one month prior Preexisting Conditions: No known chronic or long standing health conditions Allergies: No known allergies to food or medication Diagnostic Lab Data: No medical tests or lab results related to event CDC Split Type: Write-up: Patient was administered Moderna vaccine on left deltoid intramuscularly 7/12/22. Patient received incorrect dosage of 0.5 ml instead of the 0.25 ml recommended at age range. Monitored at time of vaccination for 15 minutes and patient was tolerating well. Provider informed and communicated with patient father through phone of vaccine error 7/13/22. Doctor informed father of adverse effects and recommendations, father informed doctor patient was currently stable and had gone to play. . No known adverse effects at this time. Will continue to monitor. |
|
VAERS ID: |
2367725 (history) |
Form: |
Version 2.0 |
Age: |
0.75 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2022-06-24 |
Onset: |
2022-07-06 |
Days after vaccination: |
12 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: COVID-19, Ear infection, Hypersomnia, Infant irritability, Lethargy, Pyrexia, SARS-CoV-2 test positive SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Depression (excl suicide and self injury) (broad), Neonatal disorders (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Vitamin D drops Current Illness: Ear Infection Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: COVID-19 CDC Split Type: vsafe Write-up: 06/24/2022 Vaccination 07/02/2022 Patient had an ear infection, lethargic, extended naps which is unusual for him and spiked a fever of 103.2. I called Pedicatrian. We were out of town and to give him Motrin. It went down to 101 degrees. 07/03/2022 No fever. 07/06/2022 Patient was pretty fussy that afternoon. I asked the daycare to keep eye on him if he seemed more fussier. They called me and said they think something is wrong. I went to pick up Patient. 07/06/2022 Went to Pediatrician''s office for Ear Infection. Tested POSITIVE for COVID-19. I don''t know if symptoms were due to the ear infection or COVID-19. He''s doing better with Amoxicillin and Motrin. 07/11/2022 COVID-19 NEGATIVE |
|
VAERS ID: |
2367728 (history) |
Form: |
Version 2.0 |
Age: |
1.67 |
Sex: |
Male |
Location: |
Maryland |
Vaccinated: |
2022-06-21 |
Onset: |
2022-07-03 |
Days after vaccination: |
12 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
KT9142 / 1 |
RA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Chest X-ray normal, Cough, Ear infection, Human rhinovirus test positive, Nasal congestion, Parvovirus B19 test positive, Parvovirus infection, Pyrexia, Rhinovirus infection, SARS-CoV-2 test negative, Wheezing SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Asthma/bronchospasm (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: Chest X-Ray-Normal COVID-19 Test Negative Rhino Virus- Positive Human Paraovirus- Positive CDC Split Type: vsafe Write-up: He started wheezing and having stuffy nose with a mild cough and kept on the entire week. On Sunday he had a fever all day long and got up to 103.7 and was not coming down and constantly coughing and wheezing bad. We called the on call Pediatric doctor and they suggested we go to the ER and his temperature there was 104.3. They gave him a chest X-ray and COVID-19 test and both were negative. They said he had a ear infection and offered antibiotics but we declined them. He tested positive for Rhino Virus, and Human Paraovirus. They advised to administer Ibuprofen since my wife refused the antibiotics. He has a appointment today with his regular pediatrician for follow up. |
|
VAERS ID: |
2367748 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Pennsylvania |
Vaccinated: |
2022-06-30 |
Onset: |
2022-07-08 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Induration, Injection site rash, Rash erythematous, Rash papular SMQs:, Anaphylactic reaction (broad), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: Physical exam on 7/9/22 CDC Split Type: Write-up: 8 days post-vaccination, pt developed a raised, bumpy erythematous rash at the site of the injection. ~1 in. Not itchy. Not tender. Within 24 hours, developed central clearing with underlying induration. ~1.5 inches. Not itchy. Not tender. Rash almost completely gone within 48 hours of symptom onset. NO OTHER ASSOCIATED SX. |
|
VAERS ID: |
2367752 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Connecticut |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-13 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL0007 / 1 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Incorrect product formulation administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Child vaccinated with the Pfizer formulation for children ages 5-11 and he is younger than 5 years of age. |
|
VAERS ID: |
2367783 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Minnesota |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-07 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
AR / SYR |
Administered by: Other Purchased by: ? Symptoms: Abdominal pain upper, Blood test normal, Borrelia test, Culture, Culture urine negative, Fatigue, Pyrexia, Urine output decreased SMQs:, Acute renal failure (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Constipation Preexisting Conditions: None Allergies: None Diagnostic Lab Data: Blood Culture; Urine Culture on 07/12/2022 Normal Tick/Lyme Disease Culture on 07/12/2022 Not Results Yet CDC Split Type: vsafe Write-up: On the evening of 07/07/2022 started running low grade fever from then until 07/11/2022. On 07/12/22 fever spiked up to 102.9 and the on the evening of 07/12/2022 she had stomach ache, fever up to 105.0, fatigued and low urine out put. She was taken to the ER at the Hospital and had normal blood and urine cultures. The Lyme/Tick cultures are still out and have not received the results yet. As of today she is still running a 99.0 fever. |
|
VAERS ID: |
2367798 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-13 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect product formulation administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Pt was given wrong vaccine, pt given vaccine for 5-11 year olds |
|
VAERS ID: |
2367867 (history) |
Form: |
Version 2.0 |
Age: |
0.67 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2022-06-21 |
Onset: |
2022-07-09 |
Days after vaccination: |
18 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LG / IM |
Administered by: Other Purchased by: ? Symptoms: Infant irritability, Poor feeding infant, Poor quality sleep, Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Depression (excl suicide and self injury) (broad), Neonatal disorders (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: High fever started in the middle of the night, so around 1am on July 9. Fever went as high as 102 but was kept down with ibuprofen. Baby didn''t eat well that day and she had a very rough and restless night. Still had slight fever on July 10, and very fussy, gave alternating ibuprofen and Tylenol. Nurse practitioner saw baby to confirm no ear infection. We confirmed with the 2 families we saw the week prior that nobody else had been sick. Baby had no fever and was better following day July 11. |
|
VAERS ID: |
2367891 (history) |
Form: |
Version 2.0 |
Age: |
0.92 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-10 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT914Z / 1 |
LL / IM |
Administered by: Other Purchased by: ? Symptoms: Decreased appetite, Influenza A virus test negative, Influenza B virus test, Insomnia, Irritability, Pyrexia, Rash, Somnolence, Streptococcus test negative SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: No known allergies Diagnostic Lab Data: 7/12/2022: flu swab A&B negative, strep test negative CDC Split Type: Write-up: 47 hours after receiving the shot Patient started getting a fever that lasted 48 hours in length. While he had the fever he was really sleepy during the day and then had a hard time sleeping at night. He had a poor appetite and was extremely irritable. After the fever went away he developed a rash that started on his buttocks and bilaterally on the back of his lower legs. Patient was taken to his primary care pediatrician but they did not think any treatment was necessary besides offering him whatever food or drink he would consume. |
|
VAERS ID: |
2368044 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Unknown |
Location: |
Unknown |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-13 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 2 |
- / - |
Administered by: Private Purchased by: ? Symptoms: No adverse event, Vaccination error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: NO AE - vaccine error. Patient received first dose of Moderna 6/22/22 at outside facility. Patient family did not make staff aware that they already received the first dose until after they were vaccinated again today and completed their 15min waiting period. Mom reports calling 211 and the Department of Health scheduling this appointment for the family. |
|
VAERS ID: |
2368047 (history) |
Form: |
Version 2.0 |
Age: |
0.83 |
Sex: |
Unknown |
Location: |
Unknown |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-13 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 2 |
- / - |
Administered by: Private Purchased by: ? Symptoms: Extra dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: No AE - vaccine error. Patient received first vaccine 6/22/22 at outside clinic. Patient mother did not make staff aware that the patient already received their first dose until after patient received today''s dose. Patient mom reportedly called 211 to schedule their appointment and Department of Health staff scheduled the appointment for family. |
|
VAERS ID: |
2368077 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Idaho |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-13 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FP7135 / 1 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Incorrect product formulation administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: N/A Diagnostic Lab Data: None CDC Split Type: IRIS patient ID: 769418 Write-up: Patient given adult Pfizer dose (grey cap) instead of pediatric Pfizer dose (maroon cap). |
|
VAERS ID: |
2368104 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Washington |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-07 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Extra dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: N/A CDC Split Type: Write-up: No adverse event occurred. Patient received incorrect vaccine. Patient should have received COVID-19, mRNA, LNP-S, PF, 3 mcg/0.2 mL dose, tris-sucrose (Pfizer PEDS 6m-4y (maroon). And patient received COVID-19, mRNA, LNP-S, PF, 10 mcg/0.2 mL dose, tris-sucrose (Pfizer PEDS 5y-11y (orange). |
|
VAERS ID: |
2368146 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Massachusetts |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-09 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-13 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Diarrhoea SMQs:, Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: N/A CDC Split Type: Write-up: Moderate diarrhea lasted 2 days |
|
VAERS ID: |
2368153 (history) |
Form: |
Version 2.0 |
Age: |
1.67 |
Sex: |
Female |
Location: |
Washington |
Vaccinated: |
2022-06-27 |
Onset: |
2022-07-10 |
Days after vaccination: |
13 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LL / IM |
Administered by: Public Purchased by: ? Symptoms: Diarrhoea, Fatigue, Pyrexia, SARS-CoV-2 test negative SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: Drive through COVID test (covid not detected) on 7/10/2022 CDC Split Type: Write-up: Diarrhea on 7/6 - 9:11am and 3:18pm Diarrhea on 7/8 - 4:07pm Fever 7/10 8am - 7/12 up to 102 Fatigue 7/10 - 7/12 |
|
VAERS ID: |
2368664 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
New York |
Vaccinated: |
2022-06-28 |
Onset: |
2022-07-06 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Injection site erythema, Injection site swelling, Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Multivitamin with fluoride Current Illness: Flu in May Preexisting Conditions: Beta thalassemia minor Eczema Allergies: Diagnostic Lab Data: None CDC Split Type: Write-up: Severe redness, swelling and hotness at injection site |
|
VAERS ID: |
2368781 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Massachusetts |
Vaccinated: |
2022-07-06 |
Onset: |
2022-07-14 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Injection site erythema SMQs:, Extravasation events (injections, infusions and implants) (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Redness at injection site |
|
VAERS ID: |
2368901 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Kansas |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Fatigue, Headache, Influenza virus test negative, Pyrexia, SARS-CoV-2 test negative, Streptococcus test negative SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Multivitamin Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: Strep test: negative, flu test: negative, COVID-19: negative. CDC Split Type: vsafe Write-up: Right away she did have a headache and was fatigued. The next day she seemed pretty normal. On 07/13/2022 She did come down with fatigue, a headache, low grade fever, and overall tiredness. We took her to her pediatrician the same day, they did evaluate for strep, flu, and COVID-19 and all tests came back negative. As of today she is doing completely fine and is back to her normal self. |
|
VAERS ID: |
2368959 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-10 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
6M4YPFIZER / 1 |
- / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Abdominal pain upper, Fatigue, Pyrexia, Rash, SARS-CoV-2 test negative, Urticaria SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Multivitamins Current Illness: gastroenteritis 06/25/22 Preexisting Conditions: Eczema Allergies: Cow''s milk & Egg whites Diagnostic Lab Data: Negative COVID-19 home kit 07/12/22 & 07/13/2022 CDC Split Type: Write-up: 07/10/22 - hives, stomach ache 07/11/2022 - fever, rashes, stomach ache, fatigue 07/12/2022 - low-grade fever, stomach ache, rashes 07/13/2022 - stomach ache, rashes 07/14/2022 - fever, fatigue, rashes Medications: Children''s Tylenol, Benadryl or Zyrtec, Pepto-bismol |
|
VAERS ID: |
2369003 (history) |
Form: |
Version 2.0 |
Age: |
0.83 |
Sex: |
Female |
Location: |
Oregon |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-09 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LG / IM |
Administered by: Private Purchased by: ? Symptoms: Blood test abnormal, Frustration tolerance decreased, Influenza virus test negative, Pyrexia, SARS-CoV-2 test negative, White blood cell count decreased SMQs:, Haematopoietic leukopenia (narrow), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Only what is normal from childhood vaccines. Slight fever and gone the next day or two. Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Beans and lentils Diagnostic Lab Data: COVID-19 and flu swab both negative, blood check and white cells on the low end of normal CDC Split Type: vsafe Write-up: On 07/09/2022, she started getting a fever and being frustrated. By the third day, she still had the fever and we got concerned. Took her to the doctor and they COVID-19and flu swab negative; checked her blood check and white blood count was low end of normal. So the doctor thinks it is unlikely that she has a urinary track infection. They are looking into other possibilities as to way she still has a fever. To help her with her symptoms, I gave her children''s Motrin. |
|
VAERS ID: |
2369048 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-11 |
Onset: |
2022-07-13 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Other Purchased by: ? Symptoms: Mouth swelling, Rash SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Oropharyngeal allergic conditions (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Augmentin Current Illness: ear infection Preexisting Conditions: Denies Allergies: NKDA Diagnostic Lab Data: CDC Split Type: Write-up: Generalized rash, mouth swelling began 7/13/22. Took OTC antihistamine. Prescribed steroids. |
|
VAERS ID: |
2369077 (history) |
Form: |
Version 2.0 |
Age: |
1.5 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-06-24 |
Onset: |
2022-07-02 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LL / SYR |
Administered by: Other Purchased by: ? Symptoms: Aggression, Anger, Aphonia, COVID-19, Cough, Crying, Decreased interest, Discomfort, Dysphonia, Dyspnoea, Eating disorder, Head injury, Insomnia, Irritability, Malaise, Pyrexia, Respiratory tract congestion, Rhinorrhoea, SARS-CoV-2 test positive, Screaming SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hostility/aggression (narrow), Cardiomyopathy (broad), Depression (excl suicide and self injury) (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Infant toddler multivitamin Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: At home COVID-19 test 07/05/2022 - positive; at home COVID-19 test 07/10/2022 - negative. CDC Split Type: vsafe Write-up: He started becoming sick on Saturday, and I was at the hospital having a baby at the time, so he was at my sister''s house. He wouldn''t eat and he would also have tantrums and he was acting like something was wrong. He didn''t sleep that night or the next night. He would not sleep and he was acting sick. He would not sleep or eat and was uncomfortable. When he came home on Monday on July 4, he came down with a fever. I gave him some of the infant TYLENOL and made sure he wasn''t too hot. I monitored him throughout the night. He had a runny nose and he was crying a lot. He also had the fever. I asked my sister if her daughter was sick as well, and she said no. The next day my sister had a fever and her COVID-19 test was positive. So on July 5, we all took at-home COVID-19 tests and we were all positive except my new baby. He was screaming and crying, fevers on and off for the next few days. He was really irritable, and it was really sad to see. I''m hoping that the vaccine gave him some protection. We also had to constantly suck the mucus out of his nose and almost had to take him to the hospital because he couldn''t breathe very well. We also used one of those pots to flush his nose and that helped so he could breathe again. He was mad and hitting his head on stuff. He was upset and was taking it out on me. It was horrible with him. He is getting better. We did test again on Sunday, July 10, he tested negative but he was still having symptoms. He was still having symptoms although he tested negative, so we continued to quarantine. Today, he''s still sick but he''s a lot better than he was. He''s been eating most of his meals and sleeping through the night now. He pretty much didn''t sleep through the night for maybe a week. The fevers have been gone for a while now. He also did lose his voice from crying, but he was hoarse and had no voice. He''s still sick but better than he was. And I still need to help with the runny nose and congestion. He did also cough during his infection. Basically his symptoms during the infection included coughing, congestion, runny nose, fever, tantrums, disinterest in eating and not being able to sleep. |
|
VAERS ID: |
2369197 (history) |
Form: |
Version 2.0 |
Age: |
0.5 |
Sex: |
Female |
Location: |
North Carolina |
Vaccinated: |
2022-06-22 |
Onset: |
2022-07-05 |
Days after vaccination: |
13 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: COVID-19, Cough, Fatigue, Lacrimation increased SMQs:, Anaphylactic reaction (broad), Lacrimal disorders (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: COVID-19 CDC Split Type: vsafe Write-up: She started coughing, fatigue, and had watery eyes. She was diagnosis with COVID-19. |
|
VAERS ID: |
2369431 (history) |
Form: |
Version 2.0 |
Age: |
1.17 |
Sex: |
Male |
Location: |
New Mexico |
Vaccinated: |
2022-06-28 |
Onset: |
2022-07-05 |
Days after vaccination: |
7 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR9237B / 1 |
LL / SYR |
Administered by: Other Purchased by: ? Symptoms: Agitation, Body temperature increased, Decreased appetite, Ear infection, Fatigue, Feeling hot, Rash, Rash erythematous SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: vsafe Write-up: He started feeling warm and seemed a little fussy on July 5 first thing in the morning. He started getting a higher temperature throughout the day with the highest at 101.9. He had a temperature even through part of the next day. He also started to get a rash throughout his body, and he was super tired on both days. The rash was light red dots all over his body. We went to the doctor on July 7 and saw an NP. We asked about the vaccine, and she said that it probably wasn''t in relation since it had been past 4 days. She noted that he had an ear infection as well as some kind of virus because of the rash. Because of the ear infection, she gave us a prescription for Augmentin which was 3.5 mL for 10 days twice daily. He seems fine right now. He was fine temperature wise since the 7th and the rash is gone. It was only there for about a day or two, and the ear infection has also resolved. He also did have some decreased appetite and increased tiredness during this episode of events as well. |
|
VAERS ID: |
2369443 (history) |
Form: |
Version 2.0 |
Age: |
1.75 |
Sex: |
Male |
Location: |
Texas |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-14 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LL / IM |
Administered by: Public Purchased by: ? Symptoms: Dizziness, Erythema, Pallor, Rash macular SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: NONE Allergies: NO KNOWN ALLERGIES Diagnostic Lab Data: NONE CDC Split Type: Write-up: DIZZINESS, COLOR PALLOR, BRIGHT RED SPLOCTHY SKIN . SATS WERE 97 %, PULSE 112. GAVE ICE PACKS TO BACK OF NECK.AND LOLLIPOP TO EAT. 20 MINUTES AFTER INJECTION PATIENT WAS WALKING ON HIS OWN, COLOR RETURNING TO SKIN AND NOW MORE WHITE AND PINK. MOTHER AND FATHER PRESENT, STATED "HE''S MORE LIKE HIMSELF NOW". PATIENT LEFT 30 MINUTES AFTER INJECTION WITH NO PROBLEMS. ADVISED FOLLOW WITH PEDIATRICIAN REGARDING SECOND DOSE. |
|
VAERS ID: |
2369445 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
West Virginia |
Vaccinated: |
2022-07-10 |
Onset: |
2022-07-10 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
059M21A / 1 |
LL / IM |
Administered by: Other Purchased by: ? Symptoms: Product administered to patient of inappropriate age SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: given adult dose of Moderna 0.25ml |
|
VAERS ID: |
2369485 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-06-28 |
Onset: |
2022-07-07 |
Days after vaccination: |
9 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS141B / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Abdominal pain, Cold sweat, Decreased appetite, Delirium, Fatigue, Hyperhidrosis, Hypersomnia, Injection site reaction, Irritability, Malaise, Oral pain, Oropharyngeal pain, Rash erythematous, SARS-CoV-2 test negative, Sleep disorder, Taste disorder SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Dementia (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (narrow), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (broad), Depression (excl suicide and self injury) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: Seasonal Diagnostic Lab Data: Home COVID-19 test, negative CDC Split Type: vsafe Write-up: Thursday, July 7th, I picked him up from school and walked him home. He only ate part of his fig bar because he said it didn''t taste good. He also didn''t want any dinner which is very rare. He said that his tummy hurt. I assumed it was the fig bar. He finally ate 2 bites of soup but didn''t want any more. When I brushed his teeth I only brushed half because he said it hurt. He went to bed pretty easily but he looked so exhausted. About 10:00pm he woke up and he was sweaty and clammy. He wasn''t feeling well and seemed a bit delirious because he didn''t realize I was really in the room with him as I rocked him. He cried about his tummy hurting and pointed to below his belly button. He cried and said he wanted to go home. He didn''t realize he was home. The next morning he slept in which is rare. He just wanted to keep sleeping but he needed to go to school. He didn''t want breakfast but ate some of a banana. He said it didn''t taste good. I gave him a COVID-19 test and it was negative. He said his throat hurt and he said yes. He was a bit irritable and bit whiny and then he''d be fine. After a little bit he seemed better because he was playing in the floor and went to school. At school he ate breakfast, lunch and afternoon snack and had no problems. When he got home he seemed back to normal. After I talked to the nurse mid morning, I had realized that he had a small red rash (oval size) on his arm. It was at the injection site. I messaged the doctor to let them know. |
|
VAERS ID: |
2369505 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Female |
Location: |
Washington |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-14 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LL / IM |
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
4CY9H / 1 |
LL / IM |
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
U009511 / 1 |
RL / SC |
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
U028164 / 1 |
RL / SC |
Administered by: Private Purchased by: ? Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none noted on chart Current Illness: Preexisting Conditions: 41 days in NICU- 31 6/7 weeker w/ IUGR and ASD Eye conditions/corrective lenses: 7/2021- ROP stage 1, no PLUS disease Macrocephaly Allergies: none noted on chart Diagnostic Lab Data: CDC Split Type: Write-up: Developed rash on the morning of 7/14 that spread all over body throughtout the day. |
|
VAERS ID: |
2369526 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
New York |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-14 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: The diluent was not added properly. The medical assistant said she only added 0.22 ml instead of 2.2 ml. The amount drawn and given to patient was 0.2 ml but not sure if medical assistant added diluent or if she did not add enough. |
|
VAERS ID: |
2369530 (history) |
Form: |
Version 2.0 |
Age: |
0.92 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-14 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-14 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LL / SYR |
Administered by: Private Purchased by: ? Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: No Current Illness: No Preexisting Conditions: No Allergies: No Diagnostic Lab Data: CDC Split Type: Write-up: Skin rashes all over the back, as well as the abdomal area of the patient |
|
VAERS ID: |
2370066 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Connecticut |
Vaccinated: |
2022-07-03 |
Onset: |
2022-07-03 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Circumstance or information capable of leading to medication error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: they are unsure if he got a dose; This spontaneous case was reported by a pharmacist and describes the occurrence of CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (they are unsure if he got a dose) in a 2-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. AS1414B) for COVID-19 vaccination. No Medical History information was reported. On 03-Jul-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Jul-2022, the patient experienced CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (they are unsure if he got a dose). At the time of the report, CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (they are unsure if he got a dose) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. Retired pharmacist stated that her 2 year old grandson was taken by his mother to a clinic for his 1st dose of the Moderna Covid-19 Vaccine in his right leg. As they were getting in their car about to leave that clinic, someone from the clinic stopped them & told them they are unsure if he got a dose. Caller is unsure what made them think that. They did say that they counted the doses that were given from the vial & it appears that the correct number of doses were given from it. Caller says that he hasn''t had any soreness in his right leg but that is not a good indication of whether or not he got the dose. Caller notes that his pediatrician wasn''t involved with the dose administration & that we would want to speak to the vaccination facility instead. Caller states that her daughter had spoke with the Chief Medical Officer of the vaccination facility who said they may want to consider a blood test to determine if the dose was given. No treatment medication information provided. |
|
VAERS ID: |
2370099 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Arizona |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-09 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LA / OT |
Administered by: Unknown Purchased by: ? Symptoms: Vaccination site rash SMQs:, Hypersensitivity (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: he woke up with delay onset of rash on his arm. It was pretty large, 3 inches by 2 inches of a rash where the injection site was; This spontaneous case was reported by a patient family member or friend and describes the occurrence of VACCINATION SITE RASH (he woke up with delay onset of rash on his arm. It was pretty large, 3 inches by 2 inches of a rash where the injection site was) in a 3-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On 01-Jul-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Jul-2022, the patient experienced VACCINATION SITE RASH (he woke up with delay onset of rash on his arm. It was pretty large, 3 inches by 2 inches of a rash where the injection site was). At the time of the report, VACCINATION SITE RASH (he woke up with delay onset of rash on his arm. It was pretty large, 3 inches by 2 inches of a rash where the injection site was) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient was not on any concomitant medication. Patient received first dose of the pediatric Moderna COVID-19 vaccine. Rash was not raised. It was reported that no pain from the rash. Batch/Lot number and expiration date was unknown. Patient did not received any treatment. |
|
VAERS ID: |
2370114 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Arizona |
Vaccinated: |
2022-07-11 |
Onset: |
2022-07-11 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
037A22B / 1 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Product use issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: From the 18 and up vials; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT USE ISSUE (From the 18 and up vials) in a 2-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 037A22B) for COVID-19 prophylaxis. No Medical History information was reported. On 11-Jul-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) .25 milligram. On 11-Jul-2022, the patient experienced PRODUCT USE ISSUE (From the 18 and up vials). At the time of the report, PRODUCT USE ISSUE (From the 18 and up vials) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were provided by the reporter. The vaccine was given from the vial with a red cap and light blue label border No treatment information was provided by the reporter. |
|
VAERS ID: |
2370120 (history) |
Form: |
Version 2.0 |
Age: |
0.5 |
Sex: |
Male |
Location: |
Maryland |
Vaccinated: |
2022-06-29 |
Onset: |
2022-06-30 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / UNK |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Loss of consciousness, Respiratory arrest SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypersensitivity (broad), Respiratory failure (narrow), Hypoglycaemia (broad) Life Threatening? Yes Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? Yes, ? days Extended hospital stay? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: within 24hs of getting the Moderna covdi19 vaccine patient stopped breathing; within 24hs of getting the Moderna covdi19 vaccine patient went unconscious; This spontaneous case was reported by a patient family member or friend and describes the occurrence of RESPIRATORY ARREST (within 24hs of getting the Moderna covdi19 vaccine patient stopped breathing) and LOSS OF CONSCIOUSNESS (within 24hs of getting the Moderna covdi19 vaccine patient went unconscious) in a 6-month-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. AS1414B) for COVID-19 vaccination. No Medical History information was reported. On 29-Jun-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 30-Jun-2022, the patient experienced RESPIRATORY ARREST (within 24hs of getting the Moderna covdi19 vaccine patient stopped breathing) (seriousness criteria hospitalization, medically significant and life threatening) and LOSS OF CONSCIOUSNESS (within 24hs of getting the Moderna covdi19 vaccine patient went unconscious) (seriousness criteria hospitalization and medically significant). The patient was hospitalized from sometime in 2022 to sometime in 2022 due to LOSS OF CONSCIOUSNESS and RESPIRATORY ARREST. At the time of the report, RESPIRATORY ARREST (within 24hs of getting the Moderna covdi19 vaccine patient stopped breathing) and LOSS OF CONSCIOUSNESS (within 24hs of getting the Moderna covdi19 vaccine patient went unconscious) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medication was reported. No allergies were reported. Patient never had COVID positive test or diagnosis. No Medical history was reported by the reporter. It was reported that no other vaccines were given within 1 month prior to Moderna COVID-19 vaccine. No treatment information was provided. Company Comment: This spontaneous case concerns a 6-month-old, male patient with no medical history reported, who experienced the unexpected, serious (life-threatening, hospitalization and medically significant) event of respiratory arrest and the unexpected, serious (hospitalization and medically significant) event of loss of consciousness. The events occurred within 24 hours after receiving an unspecified dose of the mRNA-1273 vaccine. It was reported that the patient stopped breathing and went unconscious, and had to be hospitalized overnight. No further clinical information (including details about hospitalization, laboratory test/s and clinical course) was available for medical review. Treatment information was also not provided. It was reported that the symptoms had improved at the time of the report. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report.; Sender''s Comments: This spontaneous case concerns a 6-month-old, male patient with no medical history reported, who experienced the unexpected, serious (life-threatening, hospitalization and medically significant) event of respiratory arrest and the unexpected, serious (hospitalization and medically significant) event of loss of consciousness. The events occurred within 24 hours after receiving an unspecified dose of the mRNA-1273 vaccine. It was reported that the patient stopped breathing and went unconscious, and had to be hospitalized overnight. No further clinical information (including details about hospitalization, laboratory test/s and clinical course) was available for medical review. Treatment information was also not provided. It was reported that the symptoms had improved at the time of the report. The benefit-risk relationship of the mRNA-1273 vaccine is not affected by this report. |
|
VAERS ID: |
2370123 (history) |
Form: |
Version 2.0 |
Age: |
1.25 |
Sex: |
Male |
Location: |
Arizona |
Vaccinated: |
2022-07-11 |
Onset: |
2022-07-11 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
037A22B / 1 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Product use issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: Patient was given injection from the presentation of the vaccine with a red cap and light blue label border; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT USE ISSUE (Patient was given injection from the presentation of the vaccine with a red cap and light blue label border) in a 15-month-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 037A22B) for COVID-19 prophylaxis. No Medical History information was reported. On 11-Jul-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 11-Jul-2022, the patient experienced PRODUCT USE ISSUE (Patient was given injection from the presentation of the vaccine with a red cap and light blue label border). At the time of the report, PRODUCT USE ISSUE (Patient was given injection from the presentation of the vaccine with a red cap and light blue label border) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was reported that the patient did not experience any symptoms. No additional doses, concomitant medications, or treatment medications had been administered. |
|
VAERS ID: |
2370130 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-06-30 |
Onset: |
2022-07-09 |
Days after vaccination: |
9 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / UNK |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Vaccination site rash SMQs:, Hypersensitivity (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: circular rash on leg at the administration site; This spontaneous case was reported by an other health care professional and describes the occurrence of VACCINATION SITE RASH (circular rash on leg at the administration site) in a 3-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On 30-Jun-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Jul-2022, the patient experienced VACCINATION SITE RASH (circular rash on leg at the administration site). At the time of the report, VACCINATION SITE RASH (circular rash on leg at the administration site) was resolving. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. It was soft and non-painful. On 11 July 2022, the rash was almost resolved. Treatment medications were not reported. |
|
VAERS ID: |
2370147 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Pennsylvania |
Vaccinated: |
2022-06-30 |
Onset: |
2022-07-08 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
RA / OT |
Administered by: Unknown Purchased by: ? Symptoms: Vaccination site erythema, Vaccination site mass, Vaccination site rash SMQs:, Hypersensitivity (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: it turned into a solid red circle/couple of little raised, red bumps around the injection site/red/by Sunday it was just a pink outline; started to develop a rash at the injection site; couple of little raised, red bumps around the injection site/raised/flat/an inch around the injection site/faded quite a bit; This spontaneous case was reported by a patient family member or friend and describes the occurrence of VACCINATION SITE RASH (started to develop a rash at the injection site), VACCINATION SITE MASS (couple of little raised, red bumps around the injection site/raised/flat/an inch around the injection site/faded quite a bit) and VACCINATION SITE ERYTHEMA (it turned into a solid red circle/couple of little raised, red bumps around the injection site/red/by Sunday it was just a pink outline) in a 2-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. AS1416B) for COVID-19 prophylaxis. No Medical History information was reported. On 30-Jun-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Jul-2022, the patient experienced VACCINATION SITE RASH (started to develop a rash at the injection site) and VACCINATION SITE MASS (couple of little raised, red bumps around the injection site/raised/flat/an inch around the injection site/faded quite a bit). On 09-Jul-2022, the patient experienced VACCINATION SITE ERYTHEMA (it turned into a solid red circle/couple of little raised, red bumps around the injection site/red/by Sunday it was just a pink outline). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency. On 11-Jul-2022, VACCINATION SITE RASH (started to develop a rash at the injection site), VACCINATION SITE MASS (couple of little raised, red bumps around the injection site/raised/flat/an inch around the injection site/faded quite a bit) and VACCINATION SITE ERYTHEMA (it turned into a solid red circle/couple of little raised, red bumps around the injection site/red/by Sunday it was just a pink outline) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant product was provided by the reporter. It was reported that it lasted for 2-3 days and he did not experience any systemic symptoms after receiving his 1st dose. |
|
VAERS ID: |
2370471 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-13 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 1 |
- / IM |
Administered by: Private Purchased by: ? Symptoms: Product preparation error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: No Current Illness: No Preexisting Conditions: No Allergies: No Diagnostic Lab Data: CDC Split Type: Write-up: Dose not diluted. |
|
VAERS ID: |
2370495 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-14 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
AR / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: DOSING ERROR: 0.5 ml was given instead of 0.25 no adverse reaction |
|
VAERS ID: |
2370496 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-14 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
AR / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Dosing error: 0.5mL given instead of 0.25mL. |
|
VAERS ID: |
2370525 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Pennsylvania |
Vaccinated: |
2022-06-23 |
Onset: |
2022-07-09 |
Days after vaccination: |
16 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
AR / SYR |
Administered by: Private Purchased by: ? Symptoms: Asthenia, COVID-19, Cough, Glassy eyes, Irritability, Pyrexia, Rhinorrhoea, SARS-CoV-2 test positive, Sneezing SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Tacrolimus; vitamin D3; cetirizine Current Illness: Prior to vaccine runny nose; cough Preexisting Conditions: Biliary Atresia; liver transplant Allergies: None Diagnostic Lab Data: COVID home test, positive CDC Split Type: vsafe Write-up: 07/10/2022 Around 2:00 PM she became super cranky, her eyes became glassy, her nose started running, she was sneezing and coughing. I tested her with a home COVID test which was positive. Her temperature was 101.5 and we called her transplant team who told us to give her TYLENOL and increase her fluids. 07/11/2022 I called her pediatrician to let them know she had tested positive. They agreed to continue her palliative care, to try a NETTY POT, and continue TYLENOL and fluids. 07/11/2022 She seemed fine. Around 3:00 PM or 4:00 PM she was out of energy. 7/12/2022 She was a little sicker that morning and her fever went up. We gave TYLENOL and she was fine for the rest of the day. 7/13/2022 she seemed fine. Yesterday she seemed a little sicker. Throughout, her nose has been very runny and she has a deep cough. She has not recovered. |
|
VAERS ID: |
2370559 (history) |
Form: |
Version 2.0 |
Age: |
1.5 |
Sex: |
Male |
Location: |
Minnesota |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Product preparation error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Tylenol, Vitamin D, iron Current Illness: none Preexisting Conditions: Allergies: nkda Diagnostic Lab Data: none CDC Split Type: Write-up: wrong diluent used to reconstitute the infant dose of Comirnaty |
|
VAERS ID: |
2370562 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Georgia |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-13 |
Days after vaccination: |
6 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: Asthenia, COVID-19, Decreased appetite, Fatigue, Pyrexia, SARS-CoV-2 test positive SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: FLINTSTONE vitamin Current Illness: Influenza B 10 days prior to vaccination Preexisting Conditions: None Allergies: None Diagnostic Lab Data: At home COVID-19 test 07/13/2022 - positive; COVID-19 PCR test 07/13/2022 - positive. CDC Split Type: vsafe Write-up: Her two most significant symptoms are fever and fatigue. It started with fatigue, and we checked for a fever at 100.7. Wednesday afternoon it was at 101.7. We gave her 5 ml of MOTRIN and went to bed at 6:15PM. The next morning, her fever was at 104 and we gave her more MOTRIN. She was very low energy and went back to sleep until about 10AM. We''ve been alternating MOTRIN and TYLENOL every 3 hours since yesterday morning. Yesterday afternoon about 4PM her fever was at 102.6. We stayed on the schedule with the medication, and she went back to bed at 6:30PM. This morning her fever was at 102.7. We gave her MOTRIN again. Her appetite wasn''t that great but she''s eating better today and had a bowel movement. She doesn''t have high energy, but she is playing today and seems to be improving. She doesn''t have a cough or much congestion. Her main symptoms are fever and fatigue. |
|
VAERS ID: |
2370566 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Washington |
Vaccinated: |
2022-07-10 |
Onset: |
2022-07-10 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AF1414B / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Cough, Fatigue, SARS-CoV-2 test positive SMQs:, Anaphylactic reaction (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Probiotics; Multivitamin Current Illness: Common Cold 6/21/2022 Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: COVID-19 rapid antigen test was negative on 07/13/2022; COVID-19 TMA-Nucleic Acid Amplification test was negative on 07/14/2022 CDC Split Type: vsafe Write-up: He experienced a cough beginning at 7pm of 07/10/2022 along with fatigue. The cough has became more frequent each day since vaccination. He has been given Zyrtec 2.5ml to try to manage the cough, and it has helped to manage the cough. The cough has remained steady, and has not resolved as of yet. |
|
VAERS ID: |
2370581 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Maryland |
Vaccinated: |
2022-06-23 |
Onset: |
2022-07-09 |
Days after vaccination: |
16 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / SYR |
Administered by: Public Purchased by: ? Symptoms: Pyrexia, SARS-CoV-2 test negative SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: 06/2022 at 2 months old she had the routine 4 different vaccines and one oral. She developed a small amount of hives after that. Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: 07-11-2022 Covid-19 Rapid Test results Negative CDC Split Type: vsafe Write-up: On Sunday night of this week she started running a fever that lasted for 36 hours. The highest fever was 102 .6. the lowest fever was about 101.1. This is 17 days after her vaccine. I did take her to her pediatrician to be tested for COVID-19 the results were negative. During that time I was giving her Tylenol and Motrin to keep her under 100 degrees. On the 07/12/2022 the fever broke that morning. |
|
VAERS ID: |
2370618 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-11 |
Days after vaccination: |
4 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / SYR |
Administered by: Private Purchased by: ? Symptoms: Decreased appetite, Listless, Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Depression (excl suicide and self injury) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Fever lasting two days that started *four days after* injection. Fever ranged between 100.5 - 101. General listlessness, loss of appetite. |
|
VAERS ID: |
2370637 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
North Carolina |
Vaccinated: |
2022-06-29 |
Onset: |
2022-07-07 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LG / IM |
Administered by: Private Purchased by: ? Symptoms: Cough, Heart rate increased, Hypopnoea, Lung disorder, Oxygen saturation decreased, Respiratory rate increased SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (narrow), Respiratory failure (narrow), Infective pneumonia (broad), Dehydration (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: gummy multivitamin (daily) Current Illness: N/A Preexisting Conditions: Allergies: Peanut allergy Diagnostic Lab Data: CDC Split Type: Write-up: Patient developed a pretty intense cough one week post vaccine around bedtime. She was able to sleep through the night fine, but when she woke up the next morning she was experiencing rapid, shallow breathing. She did not have a fever and was acting normal. When being seen by the pediatrician later that morning she was determined to have extremely tight lungs with below average O2 saturation levels and elevated heart rate. She was given back to back nebulizer treatments as well as two doses of an oral steroid at the office. She remained monitored there at the clinic for 2 hours before pediatrician determined she was safe to come home. She continued with nebulizer treatments every 4 hours for the next day and a half, then reduced to every 6 hours, then every 8 hours. She also received 4 more single doses of oral steroid daily. |
|
VAERS ID: |
2370680 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Male |
Location: |
Virginia |
Vaccinated: |
2022-06-23 |
Onset: |
2022-07-14 |
Days after vaccination: |
21 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LG / SYR |
Administered by: Other Purchased by: ? Symptoms: Irritability, Oropharyngeal pain, Pyrexia, SARS-CoV-2 test SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: MMR Vaccine 06/06/2022 age 1 - Fever a week after the vaccination Other Medications: Vitamin D Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: COVID-19 Test 07/14/2022 - Invalid CDC Split Type: vsafe Write-up: He woke up yesterday morning and he was very cranky and had a high fever. We gave him Motrin and I called the pediatrician and we got in for early afternoon. I brought him in and the Motrin had brought his fever down. She examined him and checked him for an ear infection and his throat. She noted that his throat looked a little sore and they took a nasal swab, but it came back invalid. Since he?s not in day care or anything, I didn?t plan to get him retested. Today he?s feeling a lot better. We kept up the Motrin over the night and we let that wear off and he?s doing better. He did wake up one time last night though when the Motrin wore off. At this point, his temperature seems to be normal. |
|
VAERS ID: |
2370699 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Ohio |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-15 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Fatigue, Lethargy, Tachycardia, Tachypnoea SMQs:, Anaphylactic reaction (broad), Asthma/bronchospasm (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Eosinophilic pneumonia (broad), Respiratory failure (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Dehydration (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: famotidine, Miralax, Keppra, Flovent Current Illness: bacterial rhinitis 1 month prior Preexisting Conditions: trisomy 18, laryngomalacia, IVH, ASD Allergies: NKDA Diagnostic Lab Data: None CDC Split Type: Write-up: Patient experienced tachycardia, tachypnea, extreme fatigue/lethargy, and increased oxygen demands after receiving the Moderna vaccine. Patient received vaccine the afternoon of 07/13 and 07/15 in the early morning, began to develop these symptoms. She was seen in our clinic at 10:30AM on 07/15/22 and her symptoms were improving. Will wean oxygen as tolerated at home as symptoms improve. |
|
VAERS ID: |
2370702 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
New Jersey |
Vaccinated: |
2022-06-30 |
Onset: |
2022-06-30 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
UN / UN |
Administered by: Public Purchased by: ? Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Parent denies Current Illness: Parent denies Preexisting Conditions: Allergies: NKDA reported Diagnostic Lab Data: CDC Split Type: Write-up: S/P Infant Moderna vaccine administered; approximately 15 minutes post vaccine, hives noted on face/back/arms; no tongue/ lip swelling. Lungs clear. Hives started to fade @ approximately 6:16pm w/ no additional incident Patient leaves vaccine site accompanied by parent |
|
VAERS ID: |
2370709 (history) |
Form: |
Version 2.0 |
Age: |
1.58 |
Sex: |
Female |
Location: |
Missouri |
Vaccinated: |
2022-07-06 |
Onset: |
2022-07-06 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LL / SYR |
Administered by: Private Purchased by: ? Symptoms: Vomiting SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Amoxicillin Diagnostic Lab Data: None - the nurses kept us for an additional 30 minutes of observation. They took her pulse & measured her oxygen levels. They listened to her lungs and heart. All normal and then we were released home without further incident. CDC Split Type: Write-up: After the normal observation period (15 min), patient vomited in the car on the way home. This was approximately 25 minutes after her shot. We returned immediately to the hospital. She only vomited this one time. |
|
VAERS ID: |
2370723 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
New York |
Vaccinated: |
2022-06-23 |
Onset: |
2022-07-01 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / IM |
Administered by: Unknown Purchased by: ? Symptoms: Diarrhoea, Gastroenteritis viral, Pyrexia, Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: No Current Illness: No Preexisting Conditions: None Allergies: No Diagnostic Lab Data: CDC Split Type: Write-up: Vomiting, high fever (103 F), resolved on own via Tylenol administration. 2 days post fever, diarrhea . All symptoms resolved within 4 days. We believe she had a stomach virus but was instructed by the CDC to report it anyway. |
|
VAERS ID: |
2370732 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-15 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
RA / IM |
Administered by: Unknown Purchased by: ? Symptoms: Underdose SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Client is a 2yo who moved when vaccinator went to vaccinate the child. She was pricked with the needle but no vaccine was administered. Dose discarded and new vaccine administered in other arm. |
|
VAERS ID: |
2370751 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Colorado |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-14 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: INFANTILE ECZEMA BRONCHIOLITIS Allergies: NKDA, NKFA Diagnostic Lab Data: None CDC Split Type: Write-up: Undiluted vaccine given |
|
VAERS ID: |
2370764 (history) |
Form: |
Version 2.0 |
Age: |
1.25 |
Sex: |
Male |
Location: |
Maine |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-15 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LL / IM |
DTAPIPVHIB: DTAP + IPV + HIB (PENTACEL) / SANOFI PASTEUR |
UJ613AA / 4 |
RL / IM |
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
W002596 / 1 |
LL / SC |
Administered by: Private Purchased by: ? Symptoms: Product administered to patient of inappropriate age SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Zyrtec (a few days prior, not currently) Current Illness: Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None needed. CDC Split Type: Write-up: 6-month to 4-year-old COVID-19 vaccine (dose #1) pulled from the system and entered into the medical record incorrectly as Pfizer instead of Moderna, which patient received 6/25/2022. On this basis, given COVID-19 Pfizer dose #2 in office today. After receiving the vaccine, parent asked what the course of action was, whether they needed a dose 3 in the series or not. Advised parent I would call them once I could speak with the provider. Informed provider of what happened. Contacted CDC, Pfizer manufacturer and Moderna manufacturer to determine next steps. I was directed to CDC website, where instructions where found: "Children ages 6 months to 4 years who receive different mRNA products for the first 2 doses of an mRNA COVID-19 vaccine series should follow a 3-dose schedule. A third dose of either mRNA vaccine should be administered 8 weeks after the second dose to complete the 3-dose primary series." Relayed this information to patient''s PCP, and per provider, called parent and scheduled for them to receive the Pfizer #3, 8 weeks from today. |
|
VAERS ID: |
2370767 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Florida |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-15 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Fever |
|
VAERS ID: |
2370772 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Connecticut |
Vaccinated: |
2022-06-21 |
Onset: |
2022-07-07 |
Days after vaccination: |
16 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / SYR |
Administered by: Other Purchased by: ? Symptoms: Influenza virus test negative, Lethargy, Oral disorder, Pyrexia, SARS-CoV-2 test negative, Streptococcus test negative, Viral infection SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Heart murmur (VSD) Allergies: None Diagnostic Lab Data: At home COVID-19 tests (07/07/2022) and (07/08/2022): negatives; In office COVID-19 test (07/08/2022): negative; flu and strep tests (07/08/2022): negatives. CDC Split Type: vsafe Write-up: Starting after picking her up from school, she seemed lethargic. Later, she developed a fever and was continuing to be lethargic. I gave her TYLENOL and a popsicle. I kept her from school the next day due to a mild fever. I gave her TYLENOL that evening and the next day she did not have a fever but was slightly lethargic. On 07/07/22, she tested negative on at at-home COVID-19 test. On 07/08/2022, she tested negative on another at home test. Later that day, she tested negative at the doctors office for COVID-19. I brought her to the doctor''s office solely to get the COVID test in office since its more sensitive and accurate with results. The doctor saw a few white spots in her mouth and thought she likely some virus. She tested negative also for flu and strep as well. After the doctor''s office visit, she felt fine and back to her normal self. |
|
VAERS ID: |
2370893 (history) |
Form: |
Version 2.0 |
Age: |
0.75 |
Sex: |
Male |
Location: |
Oregon |
Vaccinated: |
2022-06-29 |
Onset: |
2022-06-29 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: Diarrhoea, Ear infection, Pyrexia, SARS-CoV-2 test negative SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Loose Stools; Teething Preexisting Conditions: Chronic Ear Infection Allergies: Amoxicillin Diagnostic Lab Data: 7/11/2022- COVID-19 Test- Negative CDC Split Type: vsafe Write-up: He was having loose stools from teething. Then the day of getting the vaccine he had much larger signs of diarrhea. After that it went back down to loose teething stools. Then on 7/11/2022 he woke up with a fever. His diarrhea came back a lot worse. I took him to his doctor and they diagnosed him with another ear infection. He had no cold symptoms and everything else was fine. He has been on antibiotics for it. He is doing much better. He will be getting the ear tube surgery to prevent him from having future ear infections. This is his 6th ear infection in the last 6 months. |
|
VAERS ID: |
2371086 (history) |
Form: |
Version 2.0 |
Age: |
0.83 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-06-30 |
Onset: |
2022-07-12 |
Days after vaccination: |
12 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
A514163 / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: Body temperature increased, COVID-19, Malaise, Productive cough, Pyrexia, SARS-CoV-2 test positive, Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: vsafe Write-up: He started throwing up Tuesday morning. He spiked a temperature of about 101 degrees. I had tested positive the day before, so I called the pediatrician and they said it may just be a COVID-19 infection as well. They said to try treating the symptoms and if they got worse to go to the ER. He spent yesterday and today vomiting. He has been running fevers, so we?ve been treating that with Motrin and Tylenol. Last night he also developed a slight wet cough. The vomiting has stopped. He has a slight fever right now, but it has not gone over 100 degrees. |
|
VAERS ID: |
2371089 (history) |
Form: |
Version 2.0 |
Age: |
1.75 |
Sex: |
Female |
Location: |
Oregon |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-15 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
- / - |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Patient was erroneously given 0.2 mL dose instead of 0.25 mL dose. No adverse events were noted. |
|
VAERS ID: |
2371269 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-06 |
Onset: |
2022-07-13 |
Days after vaccination: |
7 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-15 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Injection site erythema, Injection site pruritus, Injection site rash SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: No Current Illness: No Preexisting Conditions: No Allergies: No Diagnostic Lab Data: None CDC Split Type: Write-up: Rash to right arm around vaccine site (large, red and itchy) |
|
VAERS ID: |
2371389 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2022-06-28 |
Onset: |
2022-06-29 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-16 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Generalised tonic-clonic seizure, Petit mal epilepsy, Vaccination site cellulitis, Viral rash SMQs:, Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: KEPPRA [LEVETIRACETAM] Current Illness: Seizures Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: Severe Tonic-Clonic Seizure after first dose; Absent seizures after first dose; Viral Rash after first dose; First Viral Rash after first dose; Severe Tonic-Clonic Seizure after first dose; Cellulitis at injection site after first dose; This spontaneous case was reported by a consumer and describes the occurrence of the first episode of GENERALISED TONIC-CLONIC SEIZURE (Severe Tonic-Clonic Seizure after first dose), the second episode of GENERALISED TONIC-CLONIC SEIZURE (Severe Tonic-Clonic Seizure after first dose) and PETIT MAL EPILEPSY (Absent seizures after first dose) in a 3-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. AS1416B) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Seizures. Concomitant products included LEVETIRACETAM (KEPPRA [LEVETIRACETAM]) for Seizures. On 28-Jun-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Jun-2022, the patient experienced VACCINATION SITE CELLULITIS (Cellulitis at injection site after first dose). On 01-Jul-2022, the patient experienced the first episode of GENERALISED TONIC-CLONIC SEIZURE (Severe Tonic-Clonic Seizure after first dose) (seriousness criterion medically significant) and VIRAL RASH (First Viral Rash after first dose). On 03-Jul-2022, the patient experienced PETIT MAL EPILEPSY (Absent seizures after first dose) (seriousness criterion medically significant) and VIRAL RASH (Viral Rash after first dose). On 05-Jul-2022, the patient experienced the second episode of GENERALISED TONIC-CLONIC SEIZURE (Severe Tonic-Clonic Seizure after first dose) (seriousness criterion medically significant). The patient was treated with VALPROATE SEMISODIUM (DEPAKOTE) on 06-Jul-2022 for Seizures, at an unspecified dose and frequency and CEFALEXIN (KEFLEX [CEFALEXIN]) for Cellulitis, at an unspecified dose and frequency. At the time of the report, last episode of GENERALISED TONIC-CLONIC SEIZURE (Severe Tonic-Clonic Seizure after last dose), PETIT MAL EPILEPSY (Absent seizures after first dose), VIRAL RASH (First Viral Rash after first dose), VIRAL RASH (Viral Rash after first dose) and VACCINATION SITE CELLULITIS (Cellulitis at injection site after first dose) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient was on Keppra on and off since one year old. On an unknown date in Mar-2022, the treating physician restarted Keppra. Patient had absent seizures that lasted for few seconds. Patient started Depakote for one month in addition to Keppra. company comment : This spontaneous case concerns a female child aged 3 years with relevant medical history of Seizures reported, who experienced the unexpected serious (medically significant) AESI of one episode of Generalised tonic-clonic seizure, 2nd episode of Generalised tonic-clonic seizure and unexpected serious (medically significant) event of Petit mal epilepsy that occurred after first dose of mRNA-1273 vaccination. The event one episode of Generalised tonic-clonic seizure occurred after 3 days, 2nd episode of Generalised tonic-clonic seizure occurred after 7 days and Petit mal epilepsy occurred after 5 days of vaccination. Patient had severe Tonic-Clonic Seizure on 01JUL2022 lasting for 4 minutes, absent seizures on 03JUL2022 lasting a few seconds. On 05JUL2022, she had another Tonic-Clonic Seizure lasting for 1 minute and 30 seconds. She also had two episodes of non-serious events viral rashes. She had Cellulitis at injection site treated with antibiotic Keflex. Patient was treated with Depakote to continue for 1 month in addition to Keppra LIQUID. The baby takes 4.2ml twice a day. Outcome of the events was not known at the time of report. Relevant medical history could be confounder to the events. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed as per medical judgement.; Sender''s Comments: This spontaneous case concerns a female child aged 3 years with relevant medical history of Seizures reported, who experienced the unexpected serious (medically significant) AESI of one episode of Generalised tonic-clonic seizure, 2nd episode of Generalised tonic-clonic seizure and unexpected serious (medically significant) event of Petit mal epilepsy that occurred after first dose of mRNA-1273 vaccination. The event one episode of Generalised tonic-clonic seizure occurred after 3 days, 2nd episode of Generalised tonic-clonic seizure occurred after 7 days and Petit mal epilepsy occurred after 5 days of vaccination. Patient had severe Tonic-Clonic Seizure on 01JUL2022 lasting for 4 minutes, absent seizures on 03JUL2022 lasting a few seconds. On 05JUL2022, she had another Tonic-Clonic Seizure lasting for 1 minute and 30 seconds. She also had two episodes of non-serious events viral rashes. She had Cellulitis at injection site treated with antibiotic Keflex. Patient was treated with Depakote to continue for 1 month in addition to Keppra LIQUID. The baby takes 4.2ml twice a day. Outcome of the events was not known at the time of report. Relevant medical history could be confounder to the events. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed as per medical judgement. |
|
VAERS ID: |
2371492 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-07 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-16 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
- / - |
Administered by: Other Purchased by: ? Symptoms: Lymphadenopathy, Product administered at inappropriate site, Product administered to patient of inappropriate age SMQs:, Drug abuse and dependence (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history No Allergies: Diagnostic Lab Data: CDC Split Type: USPFIZER INC202200944298 Write-up: Posterior auricular lymphadenopathy; Current age: 1 year/Lot Number: Ft9142; vaccine location Left leg; This is a spontaneous report received from non-contactable reporter(s) (Physician). A 12-month-old male patient received BNT162b2 (BNT162B2), on 07Jul2022 at 09:00 as dose 1, single (Lot number: Ft9142) at the age of 12 months, in left leg for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious) with onset 07Jul2022 at 09:00, outcome "unknown", described as "Current age: 1 year/Lot Number: Ft9142"; PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 07Jul2022 at 09:00, outcome "unknown", described as "vaccine location Left leg"; LYMPHADENOPATHY (non-serious) with onset 08Jul2022 at 21:00, outcome "not recovered", described as "Posterior auricular lymphadenopathy". Therapeutic measures were not taken as a result of lymphadenopathy. Additional information: Facility type vaccine: Doctor''s office/urgent care. The patient did not have COVID-19 prior to vaccination. The patient had not been tested post vaccination. The patient had no known allergies. |
|
VAERS ID: |
2371924 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
2022-07-16 |
Onset: |
2022-07-16 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-16 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Extra dose administered, Syringe issue SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: This was patient''s second dose. Patient accompanied by his father. Father was holding the thigh. However, the child pulled the leg when vaccinating. Content of the vaccine spilled over on his thigh. Unable to administer the vaccine. Revaccinated in the right thigh successfully. |
|
VAERS ID: |
2371929 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-16 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-16 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 2 |
- / - |
Administered by: Pharmacy Purchased by: ? Symptoms: Decreased appetite, Pyrexia, Seizure SMQs:, Torsade de pointes/QT prolongation (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Seizure, fever, loss of appetite |
|
VAERS ID: |
2371960 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Maryland |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-12 |
Days after vaccination: |
4 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-16 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Aortic dilatation, Blood glucose normal, Chest X-ray abnormal, Cough, Diarrhoea, Dyspnoea, Heart rate increased, Influenza A virus test negative, Influenza B virus test, Lung opacity, Oxygen saturation decreased, Pneumonitis, Productive cough, Respiratory distress, Respiratory syncytial virus test negative, Rhinorrhoea, SARS-CoV-2 test negative, Secretion discharge, Vomiting, Wheezing SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (broad), Asthma/bronchospasm (broad), Interstitial lung disease (narrow), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Pseudomembranous colitis (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (narrow), Hypersensitivity (broad), Noninfectious diarrhoea (narrow), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Dehydration (broad), Immune-mediated/autoimmune disorders (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? Yes Hospitalized? Yes, 1 days Extended hospital stay? No Previous Vaccinations: Other Medications: None Current Illness: 6/11/2022 she was seen at urgent care for vomiting and potential stomach bug, resolved within a day or two after. 6/29/22 she was diagnosed with a UTI that resolved after 7 days of antibiotics (Keflex). Preexisting Conditions: None Allergies: Potential but unverified allergy to amoxicillin, due to mild rash/hives one time when taking it as a younger child (Feb. 2020 or so) Diagnostic Lab Data: Urgent care tested blood sugar, normal. Negative flu, RSV, COVID at hospital. X-ray at hospital: "FINDINGS: The lungs show mild diffuse groundglass opacities bilaterally suggestive of pneumonitis without segmental consolidation or effusion. Cardiac size is normal with no vascular congestion. Aorta is insignificantly ectatic." SpO2 evening of 7/12/22 at hospital was ~94-95 awake and dipped to ~87 when asleep, prior to administration of oxygen. CDC Split Type: Write-up: Runny nose and cough beginning 7/9/22. Elevated temperature ~99.6 but never higher for a couple days. Negative PCR test for COVID on 7/10/22. On 7/12/22 she began having difficulty breathing in the morning and very rapid heartbeat along with loose stool. Taken to Pediatrics urgent care in at noon on 7/12/22 where she then vomited. Pediatrics detected pulse ox ~94 and administered zofran for the vomiting and albuterol nebulizer along with an oral steroid. Urgent care recommended transfer to the ER, and she was taken to the hospital in the late afternoon on 7/12/22. They gave additional albuterol nebulizers and continuous monitoring. At the hospital she test negative for COVID, RSV, and Flu A/B. She was admitted overnight with respiratory distress and put on low flow oxygen overnight. She responded well to the O2 oxygen and was discharged from the hospital late morning 7/13/22 with home treatment steroid and albuterol inhaler. At follow up with pediatrician on 7/14/22 vitals were good but detected wheezing, possible asthma. Prescribed 4 day course of prednisone and follow up visit. The patient is slowly getting better but with wheezy cough. The cough is now productive and discharging mucous. |
|
VAERS ID: |
2371967 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Washington |
Vaccinated: |
2022-07-16 |
Onset: |
2022-07-16 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-16 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: Rash, Rash erythematous SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: NA Current Illness: NA Preexisting Conditions: NA Allergies: NA Diagnostic Lab Data: CDC Split Type: Write-up: We took a bath and when we removed her shirt we notice 4 red rash spots on right side of upper back |
|
VAERS ID: |
2371975 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-15 |
Days after vaccination: |
14 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-16 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
03946 / 1 |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Blood test, Irritability, Laboratory test, Musculoskeletal stiffness, Pain in extremity, Seizure SMQs:, Torsade de pointes/QT prolongation (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Generalised convulsive seizures following immunisation (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: No Current Illness: No Preexisting Conditions: No Allergies: No Diagnostic Lab Data: Blood work /ok labs CDC Split Type: Write-up: Patient was fine all day then complained at about 9:00 p.m. that his arm was hurting he had no fever and didn''t want to take Tylenol. I took him up to bed with me to try to get him to sleep after some fussing he fell asleep after about 10 minutes I heard him making a strange noise he was stiff as a board and convulsing we immediately called 911 and he was taken to the ER at hospital. |
|
VAERS ID: |
2371994 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Puerto Rico |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-03 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-16 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Unknown Purchased by: ? Symptoms: Erythema, Skin papilloma SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Insect bites Diagnostic Lab Data: CDC Split Type: Write-up: It started with an eruption of reddish skin and after a few days it has warts. |
|
VAERS ID: |
2372000 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Massachusetts |
Vaccinated: |
2022-06-28 |
Onset: |
2022-06-28 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RA / IM |
Administered by: Other Purchased by: ? Symptoms: Product storage error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Error: Improper storage (ex. temp/location). |
|
VAERS ID: |
2372005 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Massachusetts |
Vaccinated: |
2022-06-24 |
Onset: |
2022-06-24 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Other Purchased by: ? Symptoms: Product storage error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Error: Improper Storage (ex. temp./location)- |
|
VAERS ID: |
2372035 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Massachusetts |
Vaccinated: |
2022-06-28 |
Onset: |
2022-06-28 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RA / IM |
Administered by: Other Purchased by: ? Symptoms: Product storage error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Error: Improper Storage (ex. temp./location)- |
|
VAERS ID: |
2372040 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Pennsylvania |
Vaccinated: |
2022-07-17 |
Onset: |
2022-07-17 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR9237B / 1 |
LL / IM |
Administered by: Other Purchased by: ? Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: ranch dressing Diagnostic Lab Data: CDC Split Type: Write-up: Hives developed around R eye 8 minutes after vaccine administration. They did not spread. No other symptoms of allergy or anaphylaxis appeared. |
|
VAERS ID: |
2372044 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-17 |
Onset: |
2022-07-17 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
- / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Melatonin 1 mg Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Was informed they gave wrong dosage. 3.7 mg instead of 3. |
|
VAERS ID: |
2372045 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Washington |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-15 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LL / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Vomiting SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Multivitamin Current Illness: None Preexisting Conditions: None Allergies: Penicillin allergy Diagnostic Lab Data: none CDC Split Type: Write-up: Vomiting - 5:30am, 6:30am, 7:30am, 8:30am, & 9:30am on Friday 7/15. One episode of vomiting Sunday 7/17 at 8:30am. |
|
VAERS ID: |
2372055 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2022-07-09 |
Onset: |
2022-07-17 |
Days after vaccination: |
8 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Rash erythematous, Rash papular, Vaccination site reaction SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None. Current Illness: Had a cold (negative PCR for Covid) prior to being vaccinated. Preexisting Conditions: No. Allergies: Cashews, pistachios, walnuts, hazelnuts, sesame. Diagnostic Lab Data: CDC Split Type: Write-up: Raised, red rash at the vaccination site eight days post-vaccination in three year old patient. Approximately 2.5 inches wide. No fever, itchiness, or pain. |
|
VAERS ID: |
2372073 (history) |
Form: |
Version 2.0 |
Age: |
1.92 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-05 |
Onset: |
2022-07-05 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Dysphonia SMQs:, Parkinson-like events (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Hoarse voice beginning day of vaccination. Peaked at day 3 and was resolved by day 7. |
|
VAERS ID: |
2372076 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Virginia |
Vaccinated: |
2022-07-02 |
Onset: |
2022-07-09 |
Days after vaccination: |
7 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-17 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / SYR |
Administered by: Private Purchased by: ? Symptoms: Joint swelling, Pain SMQs:, Haemodynamic oedema, effusions and fluid overload (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Zyrtec -5mg / daily Melatonin - 2mg / night Children''s multivitamin Current Illness: Ear infection Preexisting Conditions: Allergies: Cashews Diagnostic Lab Data: CDC Split Type: Write-up: Swollen left ankle and right knee. Minor pain |
|
VAERS ID: |
2372085 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Virginia |
Vaccinated: |
2022-06-22 |
Onset: |
2022-06-29 |
Days after vaccination: |
7 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / SYR |
Administered by: Public Purchased by: ? Symptoms: Injection site discolouration, Injection site erythema, Injection site pain, Injection site swelling, Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: MMMR vaccine (I believe) in mid left arm when he was 1.5 years old. Cellulitis developed down into his elbow. Other Medications: inhaled Budesonide 1x/daily multivitamin Current Illness: none Preexisting Conditions: bronchiopulomary dysplasia (BPD) eosinophillic esophagitis Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: He was fine until exactly 7 days post-injection when he grabbed his upper left arm and said "ow it hurts". He had a large, round red swelling greater than 3 mm in diameter, It felt hot to the touch. After it did not resolve within two days, I took him to be seen by his primary doctor''s practice. They said they thought it was an injection reaction and to treat it with ice packs and ibuprofen, which we did for a couple of days. It improved significantly that weekend. Now, three weeks later, there is only mild discoloration remaining at the injection site. |
|
VAERS ID: |
2372266 (history) |
Form: |
Version 2.0 |
Age: |
1.42 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2022-07-09 |
Onset: |
2022-07-15 |
Days after vaccination: |
6 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Rash, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Hives, flu vaccine, two times. Age 11 and 12 months Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Rash/hives on torso |
|
VAERS ID: |
2372282 (history) |
Form: |
Version 2.0 |
Age: |
0.92 |
Sex: |
Female |
Location: |
New York |
Vaccinated: |
2022-06-30 |
Onset: |
2022-07-12 |
Days after vaccination: |
12 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: COVID-19, Cough, Crying, Decreased appetite, Discomfort, Fatigue, Feeling hot, Hypophagia, Irritability, Pyrexia, Respiratory tract congestion, SARS-CoV-2 test positive, Somnolence SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Depression (excl suicide and self injury) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: MOMMY''S DROPS organic vitamin D drops Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: PCR COVID-19 test 07/12/2022 - negative; PCR COVID-19 test 07/14/2022 - positive CDC Split Type: vsafe Write-up: I tested positive during the day on Tuesday and at the time she was fine. She got very irritable and upset very easily and was crying a lot. She had a fever, a low one to begin with around 99 to 100. We called the pediatrician because she didn''t want to eat or drink for about 3 hours. We wanted to get a test done and get her seen. We saw the pediatrician on Tuesday night and her lungs were clear. She was just extra sleepy and irritable. The test was negative. She took about 3 naps a day and was napping a lot. She didn''t want to nap independently. She didn''t want to play, and she didn''t want to eat, but was still drinking breast milk and water. Thursday, she was not sleeping well and wasn''t doing too well. She was running a fever and felt very warm. She had some ibuprofen for the fever every 6 hours. She was not eating a lot but ate plain food. She was very hard to console and a lot of crying. She was just very uncomfortable. Eventually we took her back to the doctor Thursday evening and her temp was 103.8. They gave us TYLENOL in the office right away. Oxygen was okay and her lungs were clear. She was a little congested and they tested her and, she was positive. I alternated between TYLENOL and ibuprofen. Friday, we woke up and she was in the high 90s and we kept with the ibuprofen, and she was starting to move around more. She was still tired but seemed to be more normal and had a bit of a cough. This weekend she seemed more normal except being more tired and that cough. Today she''s about 90-95% but just has a little bit of coughing. |
|
VAERS ID: |
2372284 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Florida |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-14 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Electroencephalogram normal, Enterovirus test positive, Full blood count normal, Human rhinovirus test positive, Metabolic function test normal, Respiratory viral panel, Seizure like phenomena SMQs:, Convulsions (narrow), Opportunistic infections (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? Yes, 1 days Extended hospital stay? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: History of febrile seizures December 2021 and March 2022 Allergies: Diagnostic Lab Data: EEG, CBC, CMP all normal, and RVP positive for Rhino/Enterovirus CDC Split Type: Write-up: Patient had an approximate 30 second seizure like activity less than 24 hours post vaccine, followed by multiple brief seizure like events over a period of 1.5 hours.. He was afebrile. He was admitted overnight to the hospital. |
|
VAERS ID: |
2372285 (history) |
Form: |
Version 2.0 |
Age: |
0.83 |
Sex: |
Female |
Location: |
Wyoming |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-15 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 1 |
LG / IM |
Administered by: Private Purchased by: ? Symptoms: Culture urine, Pyrexia, SARS-CoV-2 test negative, Specific gravity urine increased, Urine analysis abnormal, Urine ketone body present SMQs:, Hyperglycaemia/new onset diabetes mellitus (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: COVID negative, UA showed ketones and high specific gravity, culture is pending CDC Split Type: Write-up: Fever up to 103.4 x two days |
|
VAERS ID: |
2372301 (history) |
Form: |
Version 2.0 |
Age: |
0.83 |
Sex: |
Male |
Location: |
Massachusetts |
Vaccinated: |
2022-06-24 |
Onset: |
2022-07-01 |
Days after vaccination: |
7 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LG / SYR |
Administered by: Private Purchased by: ? Symptoms: Allergy test positive, Blood test, Diarrhoea, Food allergy, Fungal infection, SARS-CoV-2 test negative, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Opportunistic infections (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Fever from flu vaccine. Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Eggs Diagnostic Lab Data: Blood work, egg allergy, COVID test, negative. CDC Split Type: vsafe Write-up: 07/01/2022 He had a yeast infection around his genital area. We took him to the doctor and he is being treated with clotrimazole. The medication cleared it all up. On 7/5/2022 there was a combination of a virus and egg allergy attack. He had diarrhea with progressively softer diarrhea from 7/5/2022 through 7/11/2022. On 7/10/2022 he had pancakes with eggs for breakfast and he broke out with hives. We took him to the emergency room. They assumed it was the virus that caused the hives. We were told to give him BENADRYL and ZYRTEC to make the hives go away. On 7/11/2022 we took him to his pediatrician. He did a COVID test which was negative. He performed a blood test and found he was allergic to eggs. He has no symptoms now. |
|
VAERS ID: |
2372316 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2022-07-18 |
Onset: |
2022-07-18 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, Product administered to patient of inappropriate age SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: N/A CDC Split Type: Write-up: Vaccine error: 5-11 year dose given to this 3 year old. No adverse event shortly after. Informed mother to watch for increase in side effects. |
|
VAERS ID: |
2372317 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
New York |
Vaccinated: |
2022-06-26 |
Onset: |
2022-06-26 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Incorrect dose administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: No adverse events reported by guardian from 6/26/2022 to 7/17/2022. CDC Split Type: Write-up: Patient came in for their second dose of Pfizer toddler primary dose series. I noticed the lot number for the first dose was a pediatric Pfizer lot number. Initially, I was not sure if it was a clerical error or an incorrect vaccine given. I notified the parent their child received pediatric Pfizer vaccine instead of toddler upon speaking to the pharmacist on duty on 6/26/2022. The pharmacist was not aware that there was a separate vial for toddler Pfizer vaccine (maroon color). The parent stated the child did not experience any side effects as a result of the first dose (pediatric dose: orange cap). Error discovered on 7/17/2022. |
|
VAERS ID: |
2372327 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2022-06-26 |
Onset: |
2022-06-26 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / UNK |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Incorrect dose administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: No adverse events reported by guardian from 6/26/22 to 7/17/22. CDC Split Type: Write-up: When patient came in for their second dose of Pfizer toddler primary dose series, I was filling out the CDC for the patient. I noticed that the lot number for the first dose was a pediatric Pfizer lot number. Initially I was not sure if it was a clerical error or an incorrect vaccine was given. I notified the parent that the child received Pediatric Pfizer vaccine instead of toddler upon speaking to the pharmacist on duty on 6/26/22. The pharmacist was not aware that there was a separate vial for toddler Pfizer vaccine (maroon color). The parent stated that the patient did not experience any side effects as a result of the first dose (pediatric dose- orange cap). Error was discovered on 7/17/22. |
|
VAERS ID: |
2372334 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2022-06-26 |
Onset: |
2022-06-26 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Incorrect product formulation administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: No adverse events reported by guardian from 6/26/22 to 7/17/22. CDC Split Type: Write-up: When patient came in for their second dose of Pfizer toddler primary dose series, I was filling out the CDC card for the patient. I noticed that the lot number for the first dose was a pediatric Pfizer lot number. Initially I was not sure if it was a clerical error or an incorrect vaccine was given. I notified the parent that the child received Pediatric Pfizer vaccine instead of toddler upon speaking to the pharmacist on duty on 6/26/22. The pharmacist was not aware that there was a separate vial for toddler Pfizer vaccine (maroon color). The parent stated that the child did not experience any side effects as a result of the first dose (pediatric dose- orange cap). Error was discovered on 7/17/22. |
|
VAERS ID: |
2372340 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
New York |
Vaccinated: |
2022-06-26 |
Onset: |
2022-06-26 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Incorrect dose administered, No adverse event, Wrong product administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: No adverse events reported by guardian from 6/26/22 to 7/17/22. CDC Split Type: Write-up: When patient came in for their second dose of Pfizer toddler primary dose series, I was filling out the CDC card for the patient. I noticed that the lot number for the first dose was a pediatric Pfizer lot number. Initially I was not sure if it was a clerical error or an incorrect vaccine was given. I notified the parent that the child received Pediatric Pfizer vaccine instead of toddler upon speaking to the pharmacist on duty on 6/26/22. The pharmacist was not aware that there was a separate vial for toddler Pfizer vaccine (maroon color). The parent stated that the child did not experience any side effects as a result of the first dose (pediatric dose- orange cap). Error was discovered on 7/17/22. |
|
VAERS ID: |
2372358 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Female |
Location: |
Michigan |
Vaccinated: |
2022-07-13 |
Onset: |
2022-07-15 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
ST9142 / 1 |
LL / SYR |
Administered by: Private Purchased by: ? Symptoms: Diarrhoea, Diarrhoea haemorrhagic, Fatigue, Irritability, Pyrexia SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal haemorrhage (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (broad), Ischaemic colitis (broad), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: COVID on July 1, 2022 Preexisting Conditions: None Allergies: None Diagnostic Lab Data: No tests CDC Split Type: vsafe Write-up: 07/15/2022 She had reports of diarrhea at daycare. That night she continued having diarrhea. Saturday morning, she had fever. The highest her fever got was 101.4. The diarrhea continued through 7/19/2022. The diarrhea had mucous and three of her movements contained blood. She was tired and irritable. She has not had no diarrhea today. She is doing pretty well now. |
|
VAERS ID: |
2372360 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Missouri |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-15 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Rash, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: CDC Split Type: Write-up: Patient noted to have new rash antecubital fossa, back of neck, behind knees, erythematous, hive like on back of neck starting approx 20 min after receiving vaccine. Given benadryl and watched for additional 15 minutes after the benadryl without changes. However, review of our clinic policy showed ER recommendation so sent to ER for extended monitoring which was normal. |
|
VAERS ID: |
2372380 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Georgia |
Vaccinated: |
2022-07-02 |
Onset: |
2022-07-13 |
Days after vaccination: |
11 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: COVID-19, Cough, Decreased appetite, Lethargy, Pyrexia, SARS-CoV-2 test positive, Somnolence SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Lisinopril; multivitamin; cefdinir Current Illness: None Preexisting Conditions: Liver and Kidney Disease Allergies: Ibuprofen because of Kidney disease Diagnostic Lab Data: Home COVID test, positive. CDC Split Type: Write-up: 07/13/2022 she woke up and was lethargic. She had a fever of 103 and a cough. She was sleepy for the rest of the day. She did not eat much, but she did drink. The next day she still had a fever but was more perky. She tested positive with a home COVID test on 7/14/2022. We gave her a dose of TYLENOL and has had none since. She has bounced back and is back to normal. |
|
VAERS ID: |
2372390 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Maryland |
Vaccinated: |
2022-06-25 |
Onset: |
2022-07-05 |
Days after vaccination: |
10 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AF1414B / 1 |
LA / IM |
Administered by: School Purchased by: ? Symptoms: Cough, Insomnia, Irritability, Pneumonia, Pyrexia, Rhinorrhoea, SARS-CoV-2 test negative SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Eosinophilic pneumonia (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (narrow), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None. Current Illness: Runny nose; cold. Preexisting Conditions: None. Allergies: None. Diagnostic Lab Data: COVID-19 test negative - 07/15/2022. CDC Split Type: vsafe Write-up: His symptoms were fever and the fever was 101-103. He had a cough, runny nose trouble sleeping, easily irritated. We took him to a doctor and they inspected him. He had mild pneumonia in his bottom left lung. They prescribed azithromycin 100mg/5ml. |
|
VAERS ID: |
2372435 (history) |
Form: |
Version 2.0 |
Age: |
0.83 |
Sex: |
Male |
Location: |
Ohio |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-16 |
Days after vaccination: |
4 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Hypophagia, Irritability, Pyrexia, SARS-CoV-2 test SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: COVID-19 test CDC Split Type: vsafe Write-up: It was Saturday but he may have been a little more fussy because mom was away. Saturday around noon dad notices the baby wouldn''t eat or drink and had fever of 101. Dad then call doctors and the doctors told him to come to the campus. No medication was given from the doctor. We were just instructed to give him Tylenol. Today he seems happy and back to normal but yesterday was pretty rough. |
|
VAERS ID: |
2372443 (history) |
Form: |
Version 2.0 |
Age: |
1.58 |
Sex: |
Female |
Location: |
South Carolina |
Vaccinated: |
2022-06-25 |
Onset: |
2022-07-13 |
Days after vaccination: |
18 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
A51414B / 1 |
RL / SYR |
Administered by: Other Purchased by: ? Symptoms: COVID-19, Irritability, Pyrexia, SARS-CoV-2 test positive, Vaccine breakthrough infection, Wheezing SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Asthma/bronchospasm (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: COVID 19 test positive. CDC Split Type: vsafe Write-up: She had a breakthrough of COVID after first dose. She had wheezing, mild fever, very fussy. |
|
VAERS ID: |
2372464 (history) |
Form: |
Version 2.0 |
Age: |
1.25 |
Sex: |
Female |
Location: |
Washington |
Vaccinated: |
2022-07-16 |
Onset: |
2022-07-16 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AF1412B / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: Runny Nose Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type: vsafe Write-up: She had a reaction in about 5 minutes of receiving. She began to have hives form on both of her arms that looked like burns. I went to the nurse and they took a look. They did call a medical emergency, gave her a shot of Benadryl in her other leg and the hives did go away very quickly within about 30 minutes. She did not have any other issues that came up and her oxygen levels were fine. She did get some hives developing on her knee however they just kept her for about an hour after the vaccine. The hives have not come back since. |
|
VAERS ID: |
2372549 (history) |
Form: |
Version 2.0 |
Age: |
0.83 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-06-25 |
Onset: |
2022-07-12 |
Days after vaccination: |
17 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
AR / IM |
Administered by: Public Purchased by: ? Symptoms: Decreased appetite, Pyrexia, Respiratory tract congestion, Rhinorrhoea, Suspected COVID-19 SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: No Current Illness: No Preexisting Conditions: No Allergies: No Diagnostic Lab Data: None CDC Split Type: vsafe Write-up: About 2 weeks after vaccination child had presumed positive for COVID-19. Had fever, runny nose, decreased appetite and congestion. Gave TYLENOL for fever. |
|
VAERS ID: |
2372559 (history) |
Form: |
Version 2.0 |
Age: |
0.75 |
Sex: |
Female |
Location: |
D.C. |
Vaccinated: |
2022-06-22 |
Onset: |
2022-07-14 |
Days after vaccination: |
22 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / SYR |
Administered by: Other Purchased by: ? Symptoms: COVID-19, Discomfort, Drainage, Feeling hot, Irritability, Pyrexia, Respiratory tract congestion, Rhinorrhoea, SARS-CoV-2 test positive SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: Vitamin D Current Illness: RSV 06/14/2022 Preexisting Conditions: None Allergies: None Diagnostic Lab Data: Rapid COVID-19 Test 07/13/2022 - Negative; PCR COVID-19 Test 07/14/2022 - Positive CDC Split Type: vsafe Write-up: She woke up on the 14th and had some sniffles. I took her to day care, and they called around 3pm and they said she had a fever of 101.7. I went and picked her up, and she was very uncomfortable, warm, and fussy. And she was having a lot of drainage from her nose. I gave her some ibuprofen and made her more comfortable. She slept through the night, and the next morning she still had congestion. It didn?t look like she had any fever that day. She has had some congestion the past few days, and that?s about it. |
|
VAERS ID: |
2372734 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Maryland |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-17 |
Days after vaccination: |
3 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
DTAPIPVHIB: DTAP + IPV + HIB (NO BRAND NAME) / SANOFI PASTEUR |
C6002BA / 5 |
LA / IM |
MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. |
U029303 / 2 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Enanthema, Induration, Nikolsky's sign, Petechiae, Rash, Rash erythematous, Rash papular, Rash pruritic, Rash vesicular, Scab, Skin lesion, Skin plaque SMQs:, Severe cutaneous adverse reactions (broad), Anaphylactic reaction (broad), Haemorrhage terms (excl laboratory terms) (narrow), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Eczema Allergies: None Diagnostic Lab Data: No tests ordered CDC Split Type: Write-up: Rapid onset, full-body rash starting 3 days after co-administration of COVID mRNA and MMRV vaccines in a healthy 4 year old male Rash is varicelliform, consisting of Indurated, vesicular, erythematous rash Several hundred lesions in total, many closely grouped, becoming confluent and forming hard plaques in several areas, especially the distal extremities Each lesion appears to start as flesh-colored or erythematous papules which grow, becoming indurated and erythematous. These then rapidly form a scab in the center of a an erythematous ring Lesions of multiple ages found in same areas Does not seem to have an ordered progression from one area to the next, i.e. not centripetal, but rather all seemed to crop up at once in multiple areas, Involves the entire body surface, worst on extremities and throat, and rather mild on trunk and scalp, but spares no surface completely It was extremely pruritic on day 1 but this seems to have abated somewhat by today (day 2) There is no oozing, crusting, bleeding, pus, or other signs of bacterial superinfection Negative Nikolsky sign and there are no areas of skin maceration Positive for enanthem consisting of petechiae on the soft palate and a few small vesicles on the soft palate and posterior pharynx Patient denies dysphagia He is otherwise very well. There is no involvement of the eyes or TMs or nasal sinuses and no significant lymphadenopathy. No fever, normal energy, no cough or rhinorrhea, no abdominal pain, no dysuria The remainder of the ROS and PE are unremarkable. |
|
VAERS ID: |
2372742 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
New Jersey |
Vaccinated: |
2022-06-24 |
Onset: |
2022-07-08 |
Days after vaccination: |
14 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: COVID-19, Cough, Exposure to SARS-CoV-2, Pyrexia, SARS-CoV-2 test positive SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: D-TAP-swollen leg-Age: 18 months. Date: Unknown. Other Medications: Children''s Multivitamin. Current Illness: Virus in early June. 06/08/2022-06/10/2022 Preexisting Conditions: None. Allergies: Peanuts; Wheat. Diagnostic Lab Data: At home COVID-19 test 07/08/22-positive CDC Split Type: vsafe Write-up: I believe my daughter was exposed to COVID-19 at camp where not everyone was masked. She came down with a high fever on 07/07/2022 but tested negative for COVID-19 with an at home test. That night she was coughing throughout the night so I retested her the next day and the results were positive. Her fever got up to 103. I reached out to her doctor who advised to give her cough syrup and to treat her fever with over the counter medication. Her fever went away for a few days by 07/12 but returned a few days later so I spoke with her pediatrician again who thought that she may have exposed to a secondary virus. At this point on 7/18/22 she is still running mild fevers at around 99 degrees. |
|
VAERS ID: |
2372751 (history) |
Form: |
Version 2.0 |
Age: |
0.75 |
Sex: |
Male |
Location: |
Nebraska |
Vaccinated: |
2022-06-26 |
Onset: |
2022-06-26 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
UNK / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Decreased appetite, Irritability, Pyrexia, Sleep disorder SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Fever found at 1600, lasted until 6/29 1700. Fever at peak was 105. Patient unable to drop fever even with administration of Motrin and Tylenol on a q 3 schedule. Loss of appetite, inability to sleep, irritability. |
|
VAERS ID: |
2372757 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Washington |
Vaccinated: |
2022-07-07 |
Onset: |
2022-07-07 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL0007 / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Product administered to patient of inappropriate age SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A. CDC Split Type: Write-up: Patient not the appropriate age for this vaccine at the time of administration. We do not know at this time if any adverse events are associated with this error. |
|
VAERS ID: |
2372781 (history) |
Form: |
Version 2.0 |
Age: |
1.42 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-17 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
- / IM |
Administered by: Private Purchased by: ? Symptoms: Erythema, Peripheral swelling SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: Had stool changes 2 days prior to vaccine. Also was diagnosed with otitis media at the end of June 2022, took augmentin for 10 days, completed course on 7/3/22. Preexisting Conditions: none Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: redness and swelling on toes and fingers |
|
VAERS ID: |
2372785 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2022-07-18 |
Onset: |
2022-07-18 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: 0.2 mL of undiluted concentrated COVID-19 vaccine for 6 months-4 yo administered. |
|
VAERS ID: |
2372788 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Wisconsin |
Vaccinated: |
2022-07-18 |
Onset: |
2022-07-18 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR9237B / 1 |
LL / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Expired product administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Patient was vaccinated with expired Moderna Toddler Vaccine. Parent brought back to repeat the dose |
|
VAERS ID: |
2372789 (history) |
Form: |
Version 2.0 |
Age: |
1.25 |
Sex: |
Female |
Location: |
North Carolina |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-15 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LL / SYR |
Administered by: Public Purchased by: ? Symptoms: Immediate post-injection reaction, Injection site erythema, Injection site swelling, Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Respiratory infection 2 weeks prior Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Immediate local reaction within 3-4 minutes with warmth, swelling, erythema. No systemic symptoms. Thigh swelling slowly resolved over 3 days |
|
VAERS ID: |
2372791 (history) |
Form: |
Version 2.0 |
Age: |
0.75 |
Sex: |
Female |
Location: |
Pennsylvania |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-17 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-18 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Rash, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Rash/Hives all over body |
|
VAERS ID: |
2372800 (history) |
Form: |
Version 2.0 |
Age: |
1.58 |
Sex: |
Male |
Location: |
Washington |
Vaccinated: |
2022-07-02 |
Onset: |
2022-07-07 |
Days after vaccination: |
5 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 1 |
LL / SYR |
Administered by: Public Purchased by: ? Symptoms: COVID-19, SARS-CoV-2 test positive SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: COVID RT pcr test CDC Split Type: Write-up: Got actual COVID infection 5 days after taking the vaccine?. |
|
VAERS ID: |
2373420 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Massachusetts |
Vaccinated: |
2022-06-23 |
Onset: |
2022-06-23 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Other Purchased by: ? Symptoms: Product storage error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Error: Improper Storage (ex. temp./location)- |
|
VAERS ID: |
2373672 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Illinois |
Vaccinated: |
2022-07-02 |
Onset: |
2022-07-03 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Arthropod bite, Erythema, Injection site reaction, Pallor, Rash erythematous, Rash papular, Rash pruritic SMQs:, Anaphylactic reaction (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Unknown Preexisting Conditions: Congenial hydronephrosis, prematurity, tethered cord, pelviectasis of the kidney, anorectal malformation Allergies: No known allergies Diagnostic Lab Data: NA CDC Split Type: Write-up: Received Pfizer COVID vaccine 7/2/22. Her mother notes that she first saw the red bumps the next day. Per mom, got "insect bites" 2 weeks ago. A few days ago they flared up after going to a water park. They were near the diaper area - four of them swelled up. She has had no fever, no illness over the past month. She describes the rash that appeared 2 days ago had spreading redness with central pallor and a red raised circular redness that is itchy. The first ones on her lateral thighs improved after using hydrocortisone topically, but other ones the next day increased. |
|
VAERS ID: |
2373699 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
New Mexico |
Vaccinated: |
2022-07-17 |
Onset: |
2022-07-17 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Joint stiffness, Lymphadenopathy, Vomiting, Wrong product administered SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Children''s Zyrtec Current Illness: none Preexisting Conditions: none Allergies: None Diagnostic Lab Data: none CDC Split Type: Write-up: We had asked for the Pfizer 6mo-5 year Covid vaccine. Instead we were given the Moderna Covid vaccine. Patient experienced vomiting, joint stiffness, swollen groin lymph nodes |
|
VAERS ID: |
2373738 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Minnesota |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LL / IM |
Administered by: Public Purchased by: ? Symptoms: Intentional medical device removal by patient SMQs: Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: inserted syringe into left thigh. Patient pulled it out before dose could be administered. Then gave full dose in right thigh(vast lat.) |
|
VAERS ID: |
2373742 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: No adverse event, Product preparation error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Maroon top Pfizer for ages 6 months through 4-year-old reconstituted incorrectly. It was reconstituted with 1.3mL versus the recommended reconstitution of 2.2mL on 07/12/2022. No adverse reaction reported. |
|
VAERS ID: |
2373744 (history) |
Form: |
Version 2.0 |
Age: |
0.92 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: No adverse event, Product preparation error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Maroon top pfizer for ages 6 months through 4 years old was reconstituted incorrectly. It was reconstituted with 1.3mL versus the recommended reconstitution of 2.2 mL on 07/12/22. No adverse reaction reported. |
|
VAERS ID: |
2373747 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: No adverse event, Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Maroon top pfizer for ages 6 months through 4 years old was reconstituted incorrectly. It was reconstituted with 1.3mL versus the recommended reconstitution of 2.2 mL on 07/12/22. No adverse reaction reported. |
|
VAERS ID: |
2373750 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Female |
Location: |
North Carolina |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, No adverse event, Product preparation issue SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Maroon top pfizer for ages 6 months through 4 years old was reconstituted incorrectly. It was reconstituted with 1.3mL versus the recommended reconstitution of 2.2 mL on 07/12/22. No adverse reaction reported. |
|
VAERS ID: |
2373752 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Delaware |
Vaccinated: |
2022-07-16 |
Onset: |
2022-07-17 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Erythema, Rash, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: CDC Split Type: Write-up: 24 hours after shot given developed hives to L leg, L back, and a few hives to R leg. Hives resolved around 36 hours after injection then reappeared on B/L legs about 54 hours after injection with erythema to B/L legs an B/L arms, all of which resolved within 8 hours. pt has never had hives or rash before. |
|
VAERS ID: |
2373768 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 2 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Inappropriate schedule of product administration SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: unknown Current Illness: unknown Preexisting Conditions: unknown Allergies: none Diagnostic Lab Data: Vitals taken after 30 minute wait. 99% oxygen, 14 rr 78 hr. Lungs clear. No signs of respiratory distress. CDC Split Type: Write-up: Patient received 2nd dose of Moderna in 2 weeks instead of 4 weeks. |
|
VAERS ID: |
2373789 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
North Carolina |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FJ4991 / UNK |
- / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: No adverse event SMQs: Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: NO Current Illness: NO Preexisting Conditions: NO Allergies: NO Diagnostic Lab Data: PATIENT HAS NOT EXPERIENCED ANY ADVERSEA EVENTS YET CDC Split Type: Write-up: PATIENT HAS NOT EXPERIENCED ANY ADVERSEA EVENTS YET |
|
VAERS ID: |
2373798 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Minnesota |
Vaccinated: |
2022-07-18 |
Onset: |
2022-07-18 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / SC |
DTAPIPV: DTAP + IPV (KINRIX) / GLAXOSMITHKLINE BIOLOGICALS |
H99J7 / 1 |
LA / IM |
MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. |
WO12741 / 1 |
RA / SC |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: patient received their covid vaccine by SubQ route instead of IM. provider informed and discussed with family |
|
VAERS ID: |
2373834 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2022-06-24 |
Onset: |
2022-06-27 |
Days after vaccination: |
3 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
UN / IM |
Administered by: Unknown Purchased by: ? Symptoms: Abdominal pain upper, Activated partial thromboplastin time, Arthralgia, Contusion, Cough, Full blood count abnormal, Henoch-Schonlein purpura, Nasopharyngitis, Palpable purpura, Platelet count increased, Prothrombin time normal, Rash, Rash erythematous, Renal function test normal, Urine analysis normal SMQs:, Anaphylactic reaction (narrow), Acute pancreatitis (broad), Haematopoietic leukopenia (broad), Haemorrhage terms (excl laboratory terms) (narrow), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vasculitis (narrow), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: unknown Current Illness: parent does not recall any illnesses in the month prior, but states was healthy during vaccination Preexisting Conditions: none Allergies: none Diagnostic Lab Data: 7/18/22 CBCd remarkable for mildly elevated platelet count. PT/PTT normal. Normal kidney function. Normal urinalysis. CDC Split Type: Write-up: Per parent of patients report: Several days after the vaccine (3-4 days), patient started developing small red bumps on legs, which eventually progressed to palpable bruises. Started having intermittent joint pains and stomach pains. Rash started to improve, then developed cough/cold symptoms, rash and the other above mentioned symptoms recurred again. I saw this patient 3 weeks and 3 days after vaccination, and based on the symptoms and clinical findings of palpable purpura, diagnosed him with Henoch Schonlein Purpura, or IgA vasculitis. He is currently undergoing symptomatic treatment with NSAIDs, fluids, and rest and not yet fully recovered. |
|
VAERS ID: |
2373842 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Florida |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-15 |
Days after vaccination: |
14 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
ST9142 / 1 |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Abnormal behaviour, Blister, COVID-19, Fatigue, Pyrexia, SARS-CoV-2 test positive, Skin exfoliation, Sleep disorder SMQs:, Severe cutaneous adverse reactions (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Psychosis and psychotic disorders (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Hostility/aggression (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Zyrtec Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: Home COVID Tests, both positive CDC Split Type: vsafe Write-up: 07/15/2022 He woke up at 3:30 in the morning with a fever of 104.3. I gave him some Ibuprofen. His temperature stayed between 102 and 104 throughout the day. I called his doctor around 11:00 am. He told me to keep the fever under control. He had no other symptoms. He had 2 home COVID tests which were both positive. The fever continued through until the next morning but broke that morning. He stayed tired, not wanting to go outside and was not being himself. This morning while taking a bath, we noticed the skin is peeling on his toes and the ball of both feet. It almost looks like a blister on one of the toes. I called the doctor and have not heard back. |
|
VAERS ID: |
2373869 (history) |
Form: |
Version 2.0 |
Age: |
0.5 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2022-07-19 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9149 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Pediarix, Rota, Prevnar given on same day Preexisting Conditions: Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: incorrect dilution . diluted with .22 |
|
VAERS ID: |
2373930 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-18 |
Onset: |
2022-07-18 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Incorrect product formulation administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Toddler, age 4, received a pediatric orange cap dose. Patient had no symptoms, but recommended to continue the series in the infant doses. |
|
VAERS ID: |
2373932 (history) |
Form: |
Version 2.0 |
Age: |
0.67 |
Sex: |
Female |
Location: |
Indiana |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-18 |
Days after vaccination: |
4 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LL / IM |
Administered by: Unknown Purchased by: ? Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: No Current Illness: None Preexisting Conditions: None Allergies: No Diagnostic Lab Data: None CDC Split Type: Write-up: Rash started on abdomen 7/18, spread to arms and legs by morning 7/19 (today) |
|
VAERS ID: |
2373949 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
2022-06-28 |
Onset: |
2022-07-01 |
Days after vaccination: |
3 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LA / IM |
Administered by: Unknown Purchased by: ? Symptoms: Hypersensitivity, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Patient returned to vaccination site 7/3/2022 for the sibling''s booster. Patient received 1st dose of PD Moderna 6/28/2022. Hives and urticaria all over the body started on 7/1/2022 (as verbalized from the mother). No outside treatment happened. No medications given by the parents. Advised to check with PCP, and provided education to the parents that no mRNA vaccine can be given in the future due to allergic reaction. |
|
VAERS ID: |
2373963 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Minnesota |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-17 |
Days after vaccination: |
3 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LG / IM |
Administered by: Private Purchased by: ? Symptoms: COVID-19, Pyrexia, SARS-CoV-2 test positive SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: Tested for COVID-19 for at the urgent care center and it was positive. CDC Split Type: vsafe Write-up: He received his COVID-19 vaccine on 07/14/2022. He didn''t show any signs of discomfort. The first signs of anything wrong was on 07/17/2022 he had a high fever. He responded well to Tylenol and Ibuprofen to break his fever. We had a telehealth visit with his doctor, they recommended that he should be seen at an urgent care center. He tested positive for COVID-19 on 07/18/2022. They recommended to keep comfortable by taking Tylenol, Ibuprofen and stay hydrated. |
|
VAERS ID: |
2374001 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Georgia |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: no Current Illness: no Preexisting Conditions: no Allergies: no Diagnostic Lab Data: CDC Split Type: Write-up: Patient given Pfizer age 5-11 10ug dose |
|
VAERS ID: |
2374157 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-15 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / N/A |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Hallucination, Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Psychosis and psychotic disorders (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: covid 7/1/2022 Preexisting Conditions: Allergies: none known Diagnostic Lab Data: CDC Split Type: Write-up: fever and hallucinations same day as vaccine, x2 days |
|
VAERS ID: |
2374242 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Expired product administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: No adverse events observed. Expired vaccine was given. The expiration time was 1448 and the vaccine was administered at 1520. |
|
VAERS ID: |
2374244 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-14 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / UNK |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Pruritus, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Sesame Diagnostic Lab Data: CDC Split Type: Write-up: Has tiny hives all over the body and super itchy hives |
|
VAERS ID: |
2374246 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Female |
Location: |
Pennsylvania |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-11 |
Days after vaccination: |
3 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142FMMJ / 1 |
UN / SYR |
Administered by: Private Purchased by: ? Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type: vsafe Write-up: 07/08/2022 Vaccination 07/11/2022 Noticed from pictures, the rash appeared on her left arm and left cheek. 07/16/2022 I noticed the rash was located on left arm, cheek and leg but no where else on her body. We called the Pediatrician office. We went to see them on Monday as it was not emergent. 07/18/2022 She had more rash on her body today. The Doctor stated there may be a connection to the vaccination, potential reaction. Over the weekend we had her on Benadryl. But now switching to Zyrtec and started today. We notice when the medication is wearing off, the rash is more prominent. The recommended Xyzal if Zyrtec doesn''t work. If it appears in joints or not her happy self, we could do a round of steroids. |
|
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-18 |
Days after vaccination: |
3 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-19 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Gait disturbance, Joint swelling, Pruritus, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Amoxicillin Current Illness: Otitis media - bilateral Preexisting Conditions: None Allergies: None known Diagnostic Lab Data: None CDC Split Type: Write-up: Patient started with urticarial rash on inner thighs on 7/18/22 (3 days after vaccination). Rash progressed over the next 24 hours and then he had swelling of bilateral wrists/ankles with refusal to walk on right foot on 7/19/22. Was also on Amoxicillin for otitis at the time of rash and mom had given dose of amoxicillin on the morning that rash began. Patient treated with Zyrtec/Benadryl for itching from rash. No fever or other systemic symptoms. |
|
VAERS ID: |
2374328 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Illinois |
Vaccinated: |
2022-07-16 |
Onset: |
2022-07-16 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LG / IM |
Administered by: Other Purchased by: ? Symptoms: Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Error: Incorrect Reconstitution- |
|
VAERS ID: |
2374666 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Massachusetts |
Vaccinated: |
2022-07-01 |
Onset: |
2022-07-02 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Full blood count, Gait disturbance, Pain in extremity, Red blood cell sedimentation rate, X-ray of pelvis and hip SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: hip XR, CbC, sed rate CDC Split Type: Write-up: Leg pain, limp |
|
VAERS ID: |
2374679 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Mississippi |
Vaccinated: |
2022-07-18 |
Onset: |
2022-07-18 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1412B / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Computerised tomogram, Electroencephalogram, Magnetic resonance imaging, Seizure, Tremor, Vomiting SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad) Life Threatening? Yes Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? Yes, ? days Extended hospital stay? No Previous Vaccinations: Other Medications: Hydrocortisone 2.5% BID PRN for eczema Current Illness: No aware of any Preexisting Conditions: Not aware of any Allergies: No known allergies Diagnostic Lab Data: Mom states that CT, MRI and EEG was performed at the local Hospital when they arrived. CDC Split Type: Write-up: Mom called and stated that at approx 10pm that child started vomiting x5 and then started shaking and have seizures shortly after. Mom reports that they then took child to nearby ED who then transferred child to a local Hospital. |
|
VAERS ID: |
2374699 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Unintentional medical device removal SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Nurse went to vaccinate child with mom holding. Child moved, needle slipped back out. No vaccine administered per RN. The administering RN changed the needle and administered the dose to the patient with both parents securing the child successfully the second attempt. |
|
VAERS ID: |
2374708 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Patient uncooperative SMQs: Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Patient presented for first Pfizer vaccine. Pt was held but twisted as vaccinator gave the vaccine and needle was withdrawn. 0.1 ml (half) of vaccine left in vial, vaccinator reports some vaccine ran down arm and therefore patient received less than 0.1 ml. Vaccine administered in opposite deltoid as ordered, specified with management and lead pharmacist. Pt was not bleeding, no adverse effects noted. Pt received vaccine as ordered, received full dose. |
|
VAERS ID: |
2374712 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Unknown |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Circumstance or information capable of leading to medication error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Nurse attempted to give vaccine with the mom holding the patient. Patient moved and the needle slipped out. No vaccine was given. RN changed the needle and safely administered full dose on the other arm with mom holding the patient securely. |
|
VAERS ID: |
2374740 (history) |
Form: |
Version 2.0 |
Age: |
1.5 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 2 |
LL / IM |
Administered by: Public Purchased by: ? Symptoms: Inappropriate schedule of product administration, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: unknown Current Illness: unknown Preexisting Conditions: unknown Allergies: none Diagnostic Lab Data: CDC Split Type: Write-up: Patient received second dose of Moderna 2 weeks after first dose. 2 weeks before they should have. Sat for 30minutes while monitored took vitals HR 98, RR 22, O2 99% RA. Lungs clear on auscultation. Instructed to call pediatrician and make an appt which family did for next day. No adverse reaction. |
|
VAERS ID: |
2374745 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-12 |
Onset: |
2022-07-12 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Interchange of vaccine products SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: unknown Current Illness: unknown Preexisting Conditions: unknown Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: Received Moderna and requested Pfizer. Monitored post 15 minutes no adverse reaction |
|
VAERS ID: |
2374771 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Georgia |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-20 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Vomiting SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Sudden onset of vomiting at 23 hours post vaccine. |
|
VAERS ID: |
2374786 (history) |
Form: |
Version 2.0 |
Age: |
1.08 |
Sex: |
Female |
Location: |
Virginia |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: Rash, Rash macular SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Children''s Benadryl Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: vsafe Write-up: Maybe thirty minutes later at home she was having a spotty rash through out her body. It was on her hands legs and on her chest. It did not seem to bother her. We do not assume it was itchy or painful. We contacted her PCP via tele conference at 05:15pm. They said to give 2ml of Children''s Benadryl. The medicine seemed to work and she went to sleep. As of today the rash is completely gone. |
|
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1412B / 2 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Emotional distress, Scratch, Syringe issue SMQs:, Accidents and injuries (narrow), Depression (excl suicide and self injury) (broad), Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Unilateral renal agenesis Allergies: No NSAIDs Diagnostic Lab Data: None CDC Split Type: Write-up: My 3 year old got his second Moderna vaccine today and he was upset and while we were trying to get him situated the nurse just quickly administered it and I felt some vaccine on my pant leg. I?m sure some was on his leg as well if there was enough to make it to my pant leg and the nurse administering it said she ?thought it was only a partial scratch? and then they ushered us out. I spoke to the doctor running the clinic and he said it was normal for some to leak out, there would most likely be a booster for him in the fall and it will end up being a 3 dose shot and that there was nothing they could do anyways as they would not revaccinate. |
|
VAERS ID: |
2374791 (history) |
Form: |
Version 2.0 |
Age: |
0.75 |
Sex: |
Female |
Location: |
Illinois |
Vaccinated: |
2022-06-30 |
Onset: |
2022-07-06 |
Days after vaccination: |
6 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LL / SYR |
Administered by: Private Purchased by: ? Symptoms: Asthenia, COVID-19, Cough, Lethargy, Pyrexia, Respiratory tract congestion, SARS-CoV-2 test positive SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: Iron Supplement Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: COVID-19 Test 07/08/2022 - Positive CDC Split Type: vsafe Write-up: On July 6, she started having a little bit of a cough. On July 7, she was not as energetic as normal. She started to seem congested. Friday the 8th, when she got up she was very lethargic. She had congestion and a cough. We took her to urgent care and she had a fever. They tested her for COVID-19 and she was positive. She was lethargic that day but ate normally. Still that cough and congestion. Saturday, her energy came back a little bit, but still coughing and congestion as well. She also did have a little bit of a fever that day. Sunday, she was going back to normal. She no longer had a fever that day. Now, she has a little bit of a cough here and there, but it''s almost gone at this point. |
|
VAERS ID: |
2374811 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Kentucky |
Vaccinated: |
2022-06-26 |
Onset: |
2022-07-12 |
Days after vaccination: |
16 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
- / IM |
Administered by: Unknown Purchased by: ? Symptoms: Enterovirus test, Illness, Magnetic resonance imaging head abnormal, Magnetic resonance imaging spinal abnormal, Myelitis transverse SMQs:, Demyelination (narrow), Immune-mediated/autoimmune disorders (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? Yes, 4 days Extended hospital stay? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: MRI brain and spine: Longitudinally extensive myelitis, most pronounced in cervical spinal cord and contiguous with posterior brainstem involvement CDC Split Type: Write-up: Transverse myelitis. Recent illness thought to be hand-foot-mouth. Also meets case definition for acute flaccid myelitis so working pt up for enteroviruses |
|
VAERS ID: |
2374812 (history) |
Form: |
Version 2.0 |
Age: |
1.5 |
Sex: |
Female |
Location: |
New York |
Vaccinated: |
2022-06-20 |
Onset: |
2022-07-19 |
Days after vaccination: |
29 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: MIRALAX Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type: vsafe Write-up: She woke up on July 19th with a fever of 101.8. No congestion and appetite good. We''ve treated fever with TYLENOL and MOTRIN. She has a low grade fever today. We reached out to our family doctor for advice. Over the weekend since my husband and I tested positive, he said to treat her as a presumed positive and treat symptoms. |
|
VAERS ID: |
2374830 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Product preparation error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: NKA Diagnostic Lab Data: CDC Split Type: Write-up: 0.2ml of unreconstituted vaccine was administered to the patient. The total number of mcg administered is unknown. The injector realized the error immediately after administration and notified the physician. There was no immediate reaction. Oral ibuprofen was administered, and the patient was observed for 2 hours. Vital signs remained stable; there was no swelling noted on her body. There was no local swelling, redness, or pain at the injection site. No rashes. An Allergist was consulted. No steroids, antihistamines, or other medications were recommended. The Hospitalist followed-up with the family in the evening, and they reported that the patient was "fine," was playing, and did not have a fever or pain. The patient''s family will be contacted daily for 3 days. |
|
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-20 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 2 |
LA / SYR |
Administered by: Public Purchased by: ? Symptoms: Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Eczema Allergies: Tree nuts Diagnostic Lab Data: None CDC Split Type: Write-up: Fever of about 102, reduced with tylenol and ibuprofen |
|
VAERS ID: |
2374892 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Oklahoma |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-15 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Abdominal pain, Body temperature increased, Culture, Dysphonia, Illness, Immunisation reaction, Incorrect dose administered, Influenza A virus test negative, Influenza B virus test, Oropharyngeal pain, Product preparation error, Streptococcus test negative, Viral infection SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Retroperitoneal fibrosis (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: Rapid strep negative. Will call if culture is positive. Flu A and B were negative. CDC Split Type: Write-up: Patient given invalid dose of COVID-19 vaccine. This was caught after being administered but prior to the patient leaving. Staff member drew-up 2.2mL of diluent in syringe with 0.2mL of vaccine and administered to the patient. Patient asked to wait 20 mins before leaving the office. Doctor spoke with the patient''s mother and advised of precautions. Spoke with Pfizer. They recommended redoing series since it was invalid, but mom and office wanted to hold-off at this time. Office visit 7/19/2022: Episode onset: 2 days ago. Maximum temperature: Temperature yesterday of 101?F - 102?F. Associated symptoms include abdominal pain and a sore throat. Pertinent negatives include no congestion, coughing, ear pain or rhinorrhea. Associated symptoms comments: Voice sounds hoarse. She tried NSAIDs for the symptoms of sore throat. Suspect viral illness or due to recent COVID-19 vaccine, though that is less likely as other family members have been ill recently. |
|
VAERS ID: |
2374894 (history) |
Form: |
Version 2.0 |
Age: |
1.08 |
Sex: |
Female |
Location: |
Illinois |
Vaccinated: |
2022-06-28 |
Onset: |
2022-07-17 |
Days after vaccination: |
19 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Hand-foot-and-mouth disease SMQs:, Oropharyngeal infections (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Fever Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Contracted hand foot and mouth disease. Diagnosed Jul 18 2022 |
|
VAERS ID: |
2374898 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Tennessee |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: no Allergies: none Diagnostic Lab Data: NA CDC Split Type: Write-up: No adverse events. Dose given was Maroon cap mixed with 1.3ml instead of 2.2ml |
|
VAERS ID: |
2374901 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Tennessee |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: No Allergies: None Diagnostic Lab Data: N/A. CDC Split Type: Write-up: No adverse events. Dose given: Maroon cap mixed with 1.3mL instead of 2.2mL. |
|
VAERS ID: |
2374911 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Minnesota |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-01 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 2 |
LA / SYR |
Administered by: Unknown Purchased by: ? Symptoms: COVID-19, Cough, Fatigue, Influenza virus test negative, Pyrexia, Respiratory syncytial virus test negative, SARS-CoV-2 test positive, Sleep disorder SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: See about above. Rapid covid PCR positive on 7/16. RSV and flu were negative. CDC Split Type: Write-up: This is too report that the VSafe info was NOT an AE. My son seemed fine the day of his second vaccine dose. Had a cough that evening. He woke up around 3am with a really bad croup-y cough, so we took him to the ER where he got a rapid PCR covid test that was positive. So all the VSafe follow-up info (fever, tired, etc) was because he had covid, and most likely not an AE to the vaccine. |
|
VAERS ID: |
2374922 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Michigan |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-20 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Injection site pain SMQs:, Extravasation events (injections, infusions and implants) (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Soreness at injection site |
|
VAERS ID: |
2374924 (history) |
Form: |
Version 2.0 |
Age: |
1.83 |
Sex: |
Male |
Location: |
Michigan |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-20 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Fever 101.4 |
|
VAERS ID: |
2374930 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Pennsylvania |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 1 |
- / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, Product administered to patient of inappropriate age SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: n/a CDC Split Type: Write-up: Wrong dosage given to patient. Patient received Pfizer age 5-11 dosage, when he should have received Pfizer age 6 month-4 year dosage. |
|
VAERS ID: |
2374953 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Arkansas |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 1 |
- / IM |
DTAPIPV: DTAP + IPV (KINRIX) / GLAXOSMITHKLINE BIOLOGICALS |
3KS4F / 1 |
- / SC |
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
U019290 / 1 |
RL / SC |
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
W003818 / 1 |
RL / SC |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: No medical test performed. CDC Split Type: Write-up: Patient is a 4-year-old male who received a 5 to 11-year-old dose of the COVID-19 vaccine. We kept him here for 30 minutes. He was monitored during this time. Patient did not experience any symptoms of an adverse reaction. He was well appearing. Vitals stable. |
|
VAERS ID: |
2374960 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-02 |
Onset: |
2022-07-11 |
Days after vaccination: |
9 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Culture positive, Rash, Staphylococcus test positive, Varicella virus test positive SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Lab confirmed Covid on 6/2/2022 Preexisting Conditions: None Allergies: None Diagnostic Lab Data: Swab results from skin rash: SP SOURCE Skin - swab VZV DNA PCR POSITIVE Abnormal ROUTINE CULT RSLT Abnormal Final Report Heavy growth Staphylococcus aureus CDC Split Type: Write-up: Patient developed a rash on his left thigh. |
|
VAERS ID: |
2374971 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Washington |
Vaccinated: |
2022-06-28 |
Onset: |
2022-07-17 |
Days after vaccination: |
19 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LA / SYR |
Administered by: Other Purchased by: ? Symptoms: COVID-19, Pyrexia, SARS-CoV-2 test positive SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Tested positive for COVID-19 on 7/17/22. Experienced fever of 103-104 for full 24 hours. (Tylenol and Ibuprofen brought it down to 102 degrees.) Next two days temperature was 100-102. Want to make it clear - the vaccine did NOT cause COVID-19 or the fever. V-safe asked for report to be submitted. |
|
VAERS ID: |
2375009 (history) |
Form: |
Version 2.0 |
Age: |
0.83 |
Sex: |
Female |
Location: |
Georgia |
Vaccinated: |
2022-06-22 |
Onset: |
2022-06-29 |
Days after vaccination: |
7 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
- / - |
Administered by: Other Purchased by: ? Symptoms: Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: No known allergies Diagnostic Lab Data: CDC Split Type: Write-up: Patient developed a fever 7 days after receiving the vaccine. The fever began mid-morning of June 29, and the her temperature was 101.8 F (measured anally) at 11:10 AM. I (patient''s mother) contacted her pediatrician''s on-call nurse line and asked what to do. They said to let the fever run its course unless she was uncomfortable or her temperature was above 102 degrees F. They said to monitor her and that they would not need to see her unless her temperature was over 102 degrees F for 24 hours, or she developed other symptoms. By 1 PM her temperature was up to 103.8 F, and I gave her one dose of infant Tylenol. This brought her temperature down to 100.4 degrees F by 2:30 PM. By 7:50 PM her temperature was back up to 103.8 degrees F. At 7:55 PM I gave her a dose of infant Motrin which brought the temperature down to 102.2 degrees F by 8:10 PM. At 8:40 PM she went to sleep for the night. On Thursday, June 30, she woke up and her temperature was slightly elevated but not a fever, at 100.2. In the afternoon she felt feverish again and I took her temperature and at 2:45 PM her temperature was back up to 102.9 degrees F. I called the nurse line at the pediatrician''s office again to ask whether they wanted to see her since her temperature had been back below 102 without medication but was back up again. They said to continue to monitor her at home for another night and treat the fever over 102 with Motrin and/or Tylenol. I gave her another dose of Motrin at 3:05 PM. Her temperature was 99.8 degrees F at 7:40 PM, so we gave her a dose of Tylenol at 7:45 PM before bed. On Friday July 1, she woke up and her temperature was 98.9 degrees F, the fever did not come back later in the day. |
|
VAERS ID: |
2375013 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Hawaii |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-20 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT142 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: No other meds on med profile. Current Illness: HEP B, HIB, POLIO Preexisting Conditions: No know health condition. Allergies: NKDA Diagnostic Lab Data: CDC Split Type: Write-up: CPhT did not dilute the vaccine with 2.2ml NaCL 0.9% and administered 0.2ml dose directly from the undiluted vaccine vial. Left a voicemail for parents to call Rx back. Will counsel patient of possible side effects. Also, will contact PCP once PCP information obtained. |
|
VAERS ID: |
2375841 (history) |
Form: |
Version 2.0 |
Age: |
1.08 |
Sex: |
Male |
Location: |
Georgia |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-21 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Vomiting SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: CDC Split Type: Write-up: vomiting about 15 hours after the vaccine. |
|
VAERS ID: |
2376586 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Male |
Location: |
Texas |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
056A22A / 1 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Unknown Current Illness: none Preexisting Conditions: none Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Given 50mcg instead of 25mcg |
|
VAERS ID: |
2376591 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
056A22A / 1 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Unknown Current Illness: none Preexisting Conditions: none Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: Patient was given 50mcg instead of 25mcg |
|
VAERS ID: |
2376592 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 2 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Wrong product administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: n/a Current Illness: n/a Preexisting Conditions: n/a Allergies: nka Diagnostic Lab Data: CDC Split Type: Write-up: Patient was given incorrect vaccine for age group. Patient received vaccine for age group 5-11yrs. No allergic reaction has been reported for patient. |
|
VAERS ID: |
2376593 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
- / - |
DTAPIPV: DTAP + IPV (KINRIX) / GLAXOSMITHKLINE BIOLOGICALS |
- / 5 |
- / - |
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
- / 2 |
- / - |
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
- / 2 |
- / - |
Administered by: School Purchased by: ? Symptoms: Wrong product administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: N/A CDC Split Type: Write-up: Patient received Pfizer 5-11yrs, no adverse event noted while observed for over 30min after administration, also nothing reported by family as of 7/21/2022 when assessed by phone 9:15am. |
|
VAERS ID: |
2376594 (history) |
Form: |
Version 2.0 |
Age: |
1.5 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 2 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Wrong product administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: n/a Current Illness: n/a Preexisting Conditions: n/a Allergies: nka Diagnostic Lab Data: CDC Split Type: Write-up: Patient was given incorrect vaccine for age group. Patient received vaccine for age group 5-11yrs. No allergic reaction has been reported for patient. |
|
VAERS ID: |
2376599 (history) |
Form: |
Version 2.0 |
Age: |
1.0 |
Sex: |
Male |
Location: |
Texas |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
056A22A / 1 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: unknown Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: Pt given 50mcg adult booster dose not 25mcg pediatric dose |
|
VAERS ID: |
2376617 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
D.C. |
Vaccinated: |
2022-06-21 |
Onset: |
2022-07-18 |
Days after vaccination: |
27 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / UNK |
RL / SYR |
Administered by: Public Purchased by: ? Symptoms: Eye swelling, Eyelid margin crusting, Periorbital swelling SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Periorbital and eyelid disorders (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Kiddie gummy vitamin Current Illness: None Preexisting Conditions: None Allergies: Amoxicillin Diagnostic Lab Data: None CDC Split Type: vsafe Write-up: 07/18/2022 that morning she woke up with a crusty, swollen and puffy right eye. We contacted her Pediatric nurse and was given a prescription for an antibiotic. The antibiotic has cleared it all up. |
|
VAERS ID: |
2376662 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Texas |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 2 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Incorrect product formulation administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Montelukast Current Illness: None Preexisting Conditions: Chronic Asthma Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Patient with DOB which is currently 4 years of age was given Pfizer (5yrs-11yrs). |
|
VAERS ID: |
2376666 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Nevada |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Circumstance or information capable of leading to medication error, Product administered to patient of inappropriate age SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: NA Current Illness: NA Preexisting Conditions: NA Allergies: NA Diagnostic Lab Data: None CDC Split Type: Write-up: The Patients parent put on the forms that patient is 5 years old. She is 4 years and 11 months. |
|
VAERS ID: |
2376682 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-21 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 2 |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Fatigue, Irritability, Pyrexia, Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Fever, vomiting, fatigue, irritability |
|
VAERS ID: |
2376704 (history) |
Form: |
Version 2.0 |
Age: |
0.92 |
Sex: |
Male |
Location: |
Missouri |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-17 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Dermatitis diaper, Diarrhoea, Fungal infection, Wound SMQs:, Pseudomembranous colitis (broad), Accidents and injuries (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Opportunistic infections (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None; formula fed Current Illness: none Preexisting Conditions: none Allergies: peanuts, eggs Diagnostic Lab Data: None CDC Split Type: Write-up: On Sunday, July 17th, pt. developed diarrhea. Due to the frequent stools, he also developed diaper rash, including open sores. As of today, July 21st, he still has diarrhea and diaper rash. 3 calls have been made to his doctor office for advice on treatment. On Monday, he started use of Lotramin cream for presumed yeast infection for topical use in area of buttocks and perineum. In addition to this Paste was applied on top of the Lotramin. On Wed, it was advised to put him on a clear liquid diet and switch to soy formula and apply milk of magnesia to diaper rash area in lieu of lotramin. After this application to apply a mixture of diaper rash cream with Zinc and cornstarch. On Thursday, due to his refusal to take soy formula, it was recommended by a doctor in his office to slowly wean him off his lactose formula and switch to Whole milk. To gradually transition off lactose while he has diarrhea. At no time did he have any other symptoms such as: fever, etc. |
|
VAERS ID: |
2376708 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
New Jersey |
Vaccinated: |
2022-07-18 |
Onset: |
2022-07-18 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Inappropriate schedule of product administration, Incorrect dose administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: History of Milk allergy and egg protein Diagnostic Lab Data: CDC Split Type: Write-up: First Covid 19 vaccination was Moderna (6 month to 5 yr dose)- given 6/27/22 Second Covid 19 vaccination Pfizer (6 month to 4 yr 11 month dose) was administered inadvertently given on 7/21/22 No adverse event |
|
VAERS ID: |
2376733 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
New Mexico |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none known Current Illness: none known Preexisting Conditions: none known Allergies: KNDA Diagnostic Lab Data: none CDC Split Type: Write-up: 1030 Pt was given incorrect dose of Pfizer vaccine (received 5-11 year old dose 0.2ml) to R thigh. RN notified. Provider notified. Pt mother notified of error and pt monitored for 30 minutes without any adverse reactions. 1107 Pt and her mother seen by MD. Pt and her mother leave clinic with no acute distress noted. |
|
VAERS ID: |
2376807 (history) |
Form: |
Version 2.0 |
Age: |
1.25 |
Sex: |
Male |
Location: |
Washington |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 2 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Vaccination error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: unknown Current Illness: unknown Preexisting Conditions: unknown Allergies: unknown Diagnostic Lab Data: unknown CDC Split Type: Write-up: Patient was present in the clinic on 7/21/2022 for his 2nd dose of Moderna (6 months ? 5yrs formulation, lot number As1414B). RN, the vaccinator, went ahead to vaccinate on the left vastus lateralis. RN''s arm moved back, and the needle left the injection site prior to vaccine administration (needle plunger has not been pressed). Vaccinator and parent were able to witness that none of the dose enter the site. RN was able to assess the site for any scratching or bruising as well assessed for any bleeding. RN notified the Charge nurse,. Parent received education on the need for repeating dose on different site (right vastus lateralis) per our protocol since none of the dose had entered the site. The parent was educated on watching the child for any bruising and that the child can be given Tylenol for comfort. Parent expressed understanding and consented to re-administration of dose in opposite site. Client was able to successfully receive dose. |
|
VAERS ID: |
2376821 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
North Carolina |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Apnoea, Unresponsive to stimuli, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Child had eruption of hives following an insect bite 1 week prior to vaccination Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Child developed hives on her face and extremities; she also had brief period of unresponsiveness (apnea). She received 02 by mask, oral benadryl (25MG) and oral prednisone (21MG). She was monitored for about 45 minutes. Her hives improved and her 02 sat remined at 100% in room air, so she was discharged home. She had another outbreak of hive about 12 hours later (at home) and was given another dose of benadryl. She has continued to take oral prednisone (21MG) to complete a 5 days course |
|
VAERS ID: |
2377051 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Colorado |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Autism Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: Medical Assistant correctly drew up 2.2 mL of normal saline to dilute the vial of vaccine. She then mistakenly administered 2.2 mL of vaccine (not 0.2 mL) to inoculate the patient. |
|
VAERS ID: |
2377070 (history) |
Form: |
Version 2.0 |
Age: |
1.08 |
Sex: |
Female |
Location: |
Georgia |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Pallor, Rash macular SMQs:, Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: blanching macular rash about 15 minutes later. mostly on trunk and some on legs/arms. no hives. |
|
VAERS ID: |
2377296 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR9237B / 2 |
RA / IM |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Incorrect dose administered, Product administered to patient of inappropriate age SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: PATIENT GOT FIRST DOSE PFIZER TODDLER AND SECOND DOSE OF MODERNA TODDLER. HE GOT MIX AND MATCH VACCINE |
|
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 2 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Extra dose administered, Product administered to patient of inappropriate age SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Patient received Pediatric Pfizer meant for ages 5years to 11 years instead of Baby Pfizer meant for ages 6months to 4 years. Patient observed for 30 minutes no adverse reaction noted. Patient /Parent informed of the vaccine the patient received. Patient /Parent advised to continue monitoring at home and to seek medical attention for any abnormalities. |
|
VAERS ID: |
2377313 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Massachusetts |
Vaccinated: |
2022-07-18 |
Onset: |
2022-07-19 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-21 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Abdominal pain, Asthenia, Chills, Decreased appetite, Headache, Lethargy, Oropharyngeal pain, Pyrexia, SARS-CoV-2 test negative, Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), COVID-19 (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: 2? red welt at vaccine site in response to seasonal flu vaccine at least twice in her life Other Medications: Claritin, fluoride supplement,s Align probiotic Current Illness: Possible COVID 2 weeks prior - never tested positive but developed an intermittent cough. Everyone else in the house had symptomatic COVID. We waited for everyone to recover and cough to fade before vaccinating her. Preexisting Conditions: Eczema, seasonal allergies Allergies: Possible fish allergy (FPIES) Diagnostic Lab Data: Home antigen COVID tests administered 7/19 and 7/21 were negative. Doctor examined child but did not think COVID PCR test nor flu test was appropriate. CDC Split Type: Write-up: Fever, chills, and lethargy rapidly developed late morning after the vaccine was administered had little appetite. Several hours later, child vomited. Fever reached over 102F and did not always respond to medicine (Tylenol and/or Motrin). Fever, chills, lethargy, lack of appetite, and intermittent belly and throat pain continued for several days. Headache developed around 1.5 days after vaccine. By 2.5 days after the vaccine, the chills/fever dissipated and energy was much improved. Throat pain remained through to day 3. No one else who was exposed to the child became ill, and the timing seems suspect, which led us to believe it was a vaccine reaction. |
|
VAERS ID: |
2379146 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Puerto Rico |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-20 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL2757 / 1 |
LA / IM |
Administered by: Other Purchased by: ? Symptoms: No adverse event, Product administered to patient of inappropriate age SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type: Write-up: The nurse in charge of vaccination at that time made an administration error; The COVID-19 vaccine was given for children between the ages of 5 to 11 years (10 mcg) instead of the vaccine for children aged 6 months to 4 years (3 mcg) that corresponded to the patient by their current age: 3 years and 9 months. Patient has not had any side effects or adverse reactions at the moment. |
|
VAERS ID: |
2379159 (history) |
Form: |
Version 2.0 |
Age: |
0.75 |
Sex: |
Male |
Location: |
Maryland |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 2 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Unevaluable event SMQs: Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Nasopharyngitis- 07/19/2022- negative covid PCR test Preexisting Conditions: None Allergies: None Diagnostic Lab Data: NONE CDC Split Type: Write-up: NONE |
|
VAERS ID: |
2379177 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-22 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 2 |
LL / SYR |
Administered by: Public Purchased by: ? Symptoms: Pyrexia, Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: N/A CDC Split Type: Write-up: Fever starting 14 hours after shot and vomiting 24 hours after shot |
|
VAERS ID: |
2379189 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Puerto Rico |
Vaccinated: |
2022-07-22 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LA / IM |
Administered by: Other Purchased by: ? Symptoms: Expired product administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: He was administered Moderna Infant vaccine, which has an expiration date today 07/22/2022 at 7:53 am. |
|
VAERS ID: |
2379195 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Pennsylvania |
Vaccinated: |
2022-07-22 |
Onset: |
2022-07-22 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR9237B / 2 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: cold approximately 2-3 weeks Preexisting Conditions: Allergies: none known Diagnostic Lab Data: none CDC Split Type: Write-up: rash developed on face, neck and LEFT arm within 5 minutes of administration, Benadryl given and rash improved within about 10 minutes |
|
VAERS ID: |
2379197 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Texas |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 1 |
RA / IM |
Administered by: Other Purchased by: ? Symptoms: Incorrect dose administered, Product administered to patient of inappropriate age SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: UNKNOWN Current Illness: UNKNOWN Preexisting Conditions: UNKNOWN Allergies: UNKNOWN Diagnostic Lab Data: UNKNOWN CDC Split Type: Write-up: CLIENT RECEIVED PEDI PFIZER FORMULATION FOR AGES 5-11YO. CLIENT WAS 4YO AT TIME OF VACCINATION AND SHOULD''VE RECEIVED 6M-4Y FORMULATION OF 3MCG/0.2ML. |
|
VAERS ID: |
2379205 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Kansas |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AR9327B / 2 |
LL / IM |
Administered by: Public Purchased by: ? Symptoms: Interchange of vaccine products SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Unknown Current Illness: None known Preexisting Conditions: None known Allergies: None Diagnostic Lab Data: None at this time CDC Split Type: Write-up: Erroneous administration of 2nd dose of Tender Age Moderna to a patient that had previously received an initial dose of Tender Age Pfizer. |
|
VAERS ID: |
2379212 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Nebraska |
Vaccinated: |
2022-07-22 |
Onset: |
2022-07-22 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Nausea, Vomiting SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: NKA Diagnostic Lab Data: None. CDC Split Type: Write-up: Nausea. Vomitted x1. |
|
VAERS ID: |
2379216 (history) |
Form: |
Version 2.0 |
Age: |
1.92 |
Sex: |
Female |
Location: |
Vermont |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-22 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / 2 |
LL / - |
Administered by: Private Purchased by: ? Symptoms: Lethargy, Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Tree nuts Diagnostic Lab Data: CDC Split Type: Write-up: Fever 103f and lethargy |
|
VAERS ID: |
2379253 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Kansas |
Vaccinated: |
2022-07-22 |
Onset: |
2022-07-22 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 2 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Incorrect dose administered, No adverse event, Product administered to patient of inappropriate age, Wrong product administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: None Known Preexisting Conditions: None Known Allergies: NKDA Diagnostic Lab Data: N/A CDC Split Type: Write-up: Patient recieved the 5-11 year old dose in error. Client was supposed to recieve the 3-4 year old dose. Patient''s mother was informed, and educated about potential for a sore arm and fever symptoms. Mother was advised to administer either tylenol or Ibuprofen before bd for the patient. Patient was monitored for 15 minutes and showed no signs of adverse reaction. |
|
VAERS ID: |
2379289 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2022-07-09 |
Onset: |
2022-07-09 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Hypersensitivity, Rash, Rash pruritic SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Patient seen due to rash immediately following first COVID vaccine (Pfizer, 6mo to 4 year dose). Pinpoint rash on arms up to shoulders. None on trunk, few on legs. Itchy but he was not scratching at them. No prior reaction to vaccines or other allergies. Benadryl given. Normal vitals, normal physical examination. Observed for 1 hour with repeat vitals and examination, again normal. Adverse reaction added to allergies. |
|
VAERS ID: |
2379324 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
Tennessee |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: CDC Split Type: Write-up: Patient was given concentrated dose of Pfizer vaccine. The vial was not diluted prior to administration. No adverse reactions noted. |
|
VAERS ID: |
2379332 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
Pennsylvania |
Vaccinated: |
2022-07-22 |
Onset: |
2022-07-22 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Product administered to patient of inappropriate age, Wrong product administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: This child came with his parents to COVID vaccine clinic to receive dose 1 of the Moderna under age 6 product. After vaccination, it was discovered that patient had received the Pediatric Pfizer (ages 5y-11y) vaccine 12/29/2021 and 01/31/2022. For those doses the parents listed the DOB as 06/29/2016 instead of 06/29/2018. The appointments in Acuity, all of the demographics including email address and home address match. The DOB is only off by the year. We pulled the paper consent from December. Both were filled out electronically and appeared identical in style and printing. The Father?s signature also appears identical. The Nurse confronted the parents and they denied this. They only wanted to prove that his DOB today is correct. The Father said ?the signatures are similar but not exactly the same?. We have canceled their dose #2 appt. |
|
VAERS ID: |
2379368 (history) |
Form: |
Version 2.0 |
Age: |
1.17 |
Sex: |
Female |
Location: |
Unknown |
Vaccinated: |
2022-06-25 |
Onset: |
2022-06-25 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
- / IM |
Administered by: Private Purchased by: ? Symptoms: Vaccination error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: NA Current Illness: NA Preexisting Conditions: Allergies: None Diagnostic Lab Data: CDC Split Type: Write-up: A 14 month old pulled away during Pediatric Covid vaccine injection. We are not sure how much of the vaccination the child received. |
|
VAERS ID: |
2379421 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Colorado |
Vaccinated: |
2022-06-22 |
Onset: |
2022-06-22 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8095 / 1 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Incorrect dose administered, Product administration error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none known Current Illness: none known Preexisting Conditions: none known Allergies: none known Diagnostic Lab Data: none known CDC Split Type: Write-up: This VAERS is to self-report a medication administration error I made 6/22/22 at approximately 16:15pm I prepared and administered 0.2 mL containing 10mcg Pfizer COVID-19 Vaccine from an orange cap vial to patient. Correct dose should have been 0.2 mL containing 3mcg Pfizer COVID=19 Vaccine from a maroon cap vial for this child. Patient: (upon clinic registration) Patient Name AKA: AGE:3Y (verified by address) DOB: (3? yrs) This patient has no history of allergies or severe allergic reactions to medication, animals or food. I contacted patient?s mother at approximately 19:24pm on my second attempt. I first asked mother how patient was doing. Mother report patient was doing just fine. I proceeded to inform mother of the medication administration error, told her patient had received the dose for a 5-year-old, and apologized for my mistake. I then reviewed the educational information regarding possible side effects and possible adverse effects which we had discussed during patient?s vaccination appointment. This includes going straight to the ER for any signs of anaphylaxis, or any deviation from common expected side effects. I encouraged mother to administer Tylenol or Ibuprofen (may alternate), as had also been discussed earlier, in efforts to keep patient comfortable. I informed her that I would be filing a report to my supervisor and to the state, but that contacting her was my first priority. Mother had asked what the difference in dosing was, and I did not have that information readily available as I was calling from home, but I would find out and get back to her. I stated that I would be calling to follow-up the next day 6/23/22, and to see how both her and the child were doing. I called 6/23/22 and 6/24/22 to follow up on the child?s well-being, without answer. I left a message both times that I would like to check in on patient and asked how she is doing. I received no return call from the parent and was unable to follow up or determine any subsequent side effects or reactions. |
|
VAERS ID: |
2379679 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-19 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
DTAPIPV: DTAP + IPV (QUADRACEL) / SANOFI PASTEUR |
C5916AA / 5 |
LL / IM |
MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. |
W007747 / 2 |
LL / SC |
Administered by: Private Purchased by: ? Symptoms: Body temperature increased, Condition aggravated, Seizure SMQs:, Torsade de pointes/QT prolongation (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: Had one previous febrile seizure Allergies: none Diagnostic Lab Data: none CDC Split Type: Write-up: Patient is a(an) 4 y.o. male who is here with parent, an additional history source. Patient had febrile seizure in May. It was associated with HFMD, had a fever and then had a seizure which was still happening when they got to the ED. He recovered. 2 nights ago he was playing video game and had a seizure that lasted 2 minutes and was generalized. He had 103 temp at the time.he got MMRV, DTaP-IPV and Pfizer COVID vaccine 8 hours prior to the seizure. After the seizure mom gave ibuprofen, he fell asleep for about 20 min, and awoke afebrile and was acting normal. He has been normal since. |
|
VAERS ID: |
2379681 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-07-22 |
Onset: |
2022-07-22 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 2 |
LL / IM |
Administered by: Other Purchased by: ? Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: eggs and nuts Diagnostic Lab Data: n/a CDC Split Type: Write-up: Patient developed hives on the face. treatment: Benadryl 12.5 mg po Outcome: Hives subsided before discharge. |
|
Vaccinated: |
2022-07-14 |
Onset: |
2022-07-14 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1412B / 2 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Inappropriate schedule of product administration SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: none CDC Split Type: Write-up: Patient was given second dose of Moderna Covid-19 vaccination 1 week too early. Given 3 weeks after first injection instead of 4 weeks. |
|
VAERS ID: |
2379690 (history) |
Form: |
Version 2.0 |
Age: |
0.58 |
Sex: |
Male |
Location: |
California |
Vaccinated: |
2022-06-24 |
Onset: |
2022-07-11 |
Days after vaccination: |
17 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
RL / SYR |
Administered by: Private Purchased by: ? Symptoms: Adverse food reaction, Erythema, Skin irritation, Skin swelling, Skin wound SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None, Tylenol and Advil as needed Current Illness: Skin abscess on buttocks Preexisting Conditions: None Allergies: No Diagnostic Lab Data: None. CDC Split Type: Write-up: Skin irritation - redness and swelling, bug bite like sores. Occurred during lunch immediately following an outdoor walk. Additionally, just bug bite sores when consuming tomatoes. Went away within 10 minutes of food being rinsed off. |
|
VAERS ID: |
2379695 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
New Jersey |
Vaccinated: |
2022-07-22 |
Onset: |
2022-07-22 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Interchange of vaccine products, No adverse event SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: None reported Preexisting Conditions: None reported Allergies: NKDA Diagnostic Lab Data: CDC Split Type: Write-up: Patient initially received first dose of infant Moderna 0.25mL on 6/24/2022. Accompanied by parent, patient received infant Pfizer 0.2mL 7/22/2022 as the second vaccine dose. No adverse reaction reported/none noted. |
|
VAERS ID: |
2379703 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
California |
Vaccinated: |
2022-07-22 |
Onset: |
2022-07-22 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL8094 / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered, No adverse event SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type: Write-up: Administered a 5-11 pfizer vaccine to a 3y.o. on left deltoid at 14:50 on 7/22/22. Patient was monitored for 30 minutes and presenting with no adverse reactions. Physician assessed patient and informed guardians about possible side effects. After observation period, patient was assessed for any allergic reactions. Patient reported "feeling fine" and guardian confirmed patient was doing well after observation period. |
|
VAERS ID: |
2379718 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Illinois |
Vaccinated: |
2022-07-19 |
Onset: |
2022-07-20 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-22 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
UN / IM |
Administered by: Public Purchased by: ? Symptoms: Full blood count normal, Metabolic function test, Rash, Red blood cell sedimentation rate normal, Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: Congestion and runny nose Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CBC, BMP, and sed rate within normal limits. An EBV and mycoplasma are pending. Performed 7/22/22. CDC Split Type: Write-up: Child developed hives on face on Wednesday morning, 7/20/22, 1 day following receiving Covid19 vaccination. By Thursday evening, 7/21/22, patient was covered from head to toe in hives. Patient was evaluated in clinic On Friday, 7/22/22, and noted to have rash consistent with urticaria multiforme. Mother was instructed to use antihistamine and topical steroid for symptom relief. |
|
VAERS ID: |
2381839 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2022-07-22 |
Onset: |
2022-07-22 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
LG / IM |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LG / IM |
Administered by: Private Purchased by: ? Symptoms: Pain in extremity, Peripheral swelling, Sleep disorder SMQs:, Cardiac failure (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Tendinopathies and ligament disorders (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Both vaccines son woke at 12pm, could not sleep for 2.5 hours. Happy but would not sleep. Only two times in his life it''s happened Also, post second vaccine, he''s swollen. Feet and hands are red and swollen, can''t walk without saying ou Current Illness: Cold Preexisting Conditions: Possible reactive airway Allergies: Lanolin oil Diagnostic Lab Data: CDC Split Type: Write-up: Night waking Swelling in hands, feet and ankles. Legs not weight baring without pain |
|
VAERS ID: |
2383848 (history) |
Form: |
Version 2.0 |
Age: |
1.25 |
Sex: |
Male |
Location: |
New York |
Vaccinated: |
2022-07-20 |
Onset: |
2022-07-22 |
Days after vaccination: |
2 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
80777-279-05 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Irritability, Rash SMQs:, Anaphylactic reaction (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Global rash and extreme irritablity thus far. |
|
VAERS ID: |
2383850 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
New York |
Vaccinated: |
2022-07-23 |
Onset: |
2022-07-23 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
A51414B / 1 |
LL / IM |
Administered by: Other Purchased by: ? Symptoms: Hyperhidrosis, Pallor SMQs:, Neuroleptic malignant syndrome (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? Yes Hospitalized? No Previous Vaccinations: Other Medications: n/a Current Illness: n/a Preexisting Conditions: n/a Allergies: nkda Diagnostic Lab Data: CDC Split Type: Write-up: Vaccine site without AC, 90F at time of incident. Pt became pale and diaphoretic approximately 5 minutes after covid vaccination, during 15 min observation period. Vital signs stable, pt showing no signs of anaphylaxis or allergic reaction. 911 called at 10:05am for further evaluation, called again at 10:14am. EMS arrived at 10:16am and took over care. Pt transferred via EMS to a local Hospital for further eval/observation. |
|
VAERS ID: |
2384567 (history) |
Form: |
Version 2.0 |
Age: |
0.83 |
Sex: |
Male |
Location: |
South Carolina |
Vaccinated: |
2022-07-21 |
Onset: |
2022-07-21 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: C-reactive protein increased, Carbon dioxide decreased, Erythema multiforme, Full blood count abnormal, Leukocytosis, Malaise, Metabolic acidosis, Metabolic function test, Metabolic function test abnormal, Pyrexia, Rash, Rash erythematous, Rash pruritic, White blood cell count increased SMQs:, Severe cutaneous adverse reactions (narrow), Anaphylactic reaction (broad), Haematopoietic leukopenia (broad), Lactic acidosis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Chronic kidney disease (broad), Hypersensitivity (narrow), Tumour lysis syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (narrow), Immune-mediated/autoimmune disorders (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? Yes ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Amoxicillin Current Illness: acute otits media 7/12/22 (was on amox day #9 at time of covid #2) Preexisting Conditions: none Allergies: nkda Diagnostic Lab Data: CBC showed leukocytosis, WBC 15.8, CMP showed mild metabolic acidosis (CO2 16), otherwise within normal limits. CRP elevated 93.4 mg/L CDC Split Type: Write-up: Rash onset within hours of vaccination on 7/21/22 with itchy red bumps, progressed over 2 days to widespread cutaneous erythema multiforme (approx 30% BSA), fever, malaise. No mucosal involvement, no sloughing when examined on 7/23/22. D/w pediatric infectious disease specialist, decided to closely monitor outpatient, start oral steroids. Note: maternal hx SJS, suspect genetic predisposition, but no HLA subtyping done to date |
|
VAERS ID: |
2385001 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Virginia |
Vaccinated: |
2022-07-23 |
Onset: |
2022-07-23 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 1 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Agitation, Rash SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: None reported by father during pre-vaccination screening. Diagnostic Lab Data: CDC Split Type: Write-up: ? 0940-Child vaccinated with 1st dose Pediatric Pfizer COVID 19 Vaccine(6 months-4years) in right vastus lateralis by RN. Child extremely agitated before and during vaccination. ? 1000-Dad noticed rash on thighs and SO notified by OBS staff. ? Non-raised rash noted by SO on bilateral thighs and anterior/posterior trunk. ? No swelling of lips, no hives, color pink, child in NAD, bilateral BS nl, no wheezing, moving air bilaterally without difficulty, awake and alert. "Acting normal" per dad. ? Dad declined EMS activation. SO requested dad to stay additional OBS time for total of 30 minutes and to notify OBS staff of any change in child''s condition. ? 1015-Dad ready to leave OBS. ? SO assessment at this time: rash-no change. ? Child in NAD, color nl, no swelling noted, no hives, bilateral BS nl, no wheezing, moving air bilaterally without difficulty. ? Instructed father in s/s anaphylactic rxn and potential latent rxn, contact 911 if s/s respiratory distress/swelling of lips/tongue, contact PCP with any other concerns post-vaccination. Dad verbalized understanding of all instructions and says he would like to continue to monitor child at home at this time. ? Child awake and alert, carried by dad from vaccination clinic @1020. |
|
VAERS ID: |
2385010 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Louisiana |
Vaccinated: |
2022-07-17 |
Onset: |
2022-07-17 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
RL / IM |
Administered by: Other Purchased by: ? Symptoms: Syringe issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Error: Leaking from Syringe- |
|
VAERS ID: |
2385360 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Maryland |
Vaccinated: |
2022-07-23 |
Onset: |
2022-07-23 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1412B / 2 |
RL / IM |
Administered by: Public Purchased by: ? Symptoms: Circumstance or information capable of leading to medication error, Scratch, Underdose SMQs:, Accidents and injuries (narrow), Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? Yes Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: food Diagnostic Lab Data: none CDC Split Type: Write-up: Dad came with child for child''s 2nd dose Moderna 0.25ml. Dad sat with child on his lap, child was already very anxious . Asked his dad which site to give vaccine he said thigh, I asked if right thigh was ok he said yes. I asked dad to hold the child''s hands. I cleaned the right thigh. I got off my chair to give the vaccine, I held the thigh as I was administering the vaccine the child moved his leg, all of the vaccine spilled out and the needle scratched the thigh. Cleaned the area and applied the bandaid no distress noted. Supervisor notified. Offered to give repeat dose but Dad declined stated child is already anxious. Dad was advised to reschedule. |
|
VAERS ID: |
2386219 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
North Carolina |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-15 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
014B22A / 1 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: This spontaneous case was reported by a medical assistant and describes the occurrence of INCORRECT DOSE ADMINISTERED (Pediatric patient of age 2 year 11 months old received first dose 0.25ml from Red Cap adult vial) in a 2-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 014B22A) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Jul-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 15-Jul-2022, the patient experienced INCORRECT DOSE ADMINISTERED (Pediatric patient of age 2 year 11 months old received first dose 0.25ml from Red Cap adult vial). At the time of the report, INCORRECT DOSE ADMINISTERED (Pediatric patient of age 2 year 11 months old received first dose 0.25ml from Red Cap adult vial) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient''s age reported as 2 year 11 months old. No concomitant medications were reported. No treatment details were reported. It was reported that the patient received Moderna COVID-19 Vaccine dose of 0.25 ml from a vial with red cap and a label with light blue border with order number NDC: 80777-273-10. Reporter already notified the health department. |
|
VAERS ID: |
2386842 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Colorado |
Vaccinated: |
2022-07-22 |
Onset: |
2022-07-22 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LL / IM |
Administered by: Public Purchased by: ? Symptoms: Hypersensitivity, Injection site erythema, Injection site rash, Injection site warmth SMQs:, Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: NKA Diagnostic Lab Data: NA CDC Split Type: Write-up: The patient''s mother informed my team lead of an allergic reaction. The patient developed a rash on her left, lateral, lower leg. The rash was warm to touch with red, raised bumps. The child was not in distress, she had no pain and responded no when asked if it itched. After doing a head to toe exam, I found the patient was A/Ox3, PMS x3 and airway was open. The patient was administered (1) children''s chewable benadryl. The mother was advised to follow up with a pediatrician and monitor her child for any other developing symptoms. |
|
VAERS ID: |
2386881 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Male |
Location: |
Kansas |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LL / OT |
Administered by: Unknown Purchased by: ? Symptoms: Product preparation error, Underdose SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Comments: Patient did not had any allergies related to food, medications and other products. Patient had tested positive for Covid-19. Patient did not had any acute illness at the time of vaccination and up to one month before. Patient did not had any chronic or long standing health conditions. Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: The vaccine was administered after being diluted by the Pfizer COVID-19 vaccine diluent, 2.2 mL of 0.9% sodium chloride (normal saline, preservative free) of the diluent used for Pfizer COVID-19 vaccine into the bottle of magenta border Moderna; vaccine was administered, 0.2 mL dose and administered to 3 year 2 month child; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT PREPARATION ERROR (The vaccine was administered after being diluted by the Pfizer COVID-19 vaccine diluent, 2.2 mL of 0.9% sodium chloride (normal saline, preservative free) of the diluent used for Pfizer COVID-19 vaccine into the bottle of magenta border Moderna) and UNDERDOSE (vaccine was administered, 0.2 mL dose and administered to 3 year 2 month child) in a 3-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. AS1416B) for COVID-19 prophylaxis. Patient did not had any allergies related to food, medications and other products. Patient had tested positive for Covid-19. Patient did not had any acute illness at the time of vaccination and up to one month before. Patient did not had any chronic or long standing health conditions. On 08-Jul-2022 at 8:00 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .2 milliliter. On 08-Jul-2022 at 8:00 AM, the patient experienced UNDERDOSE (vaccine was administered, 0.2 mL dose and administered to 3 year 2 month child). On an unknown date, the patient experienced PRODUCT PREPARATION ERROR (The vaccine was administered after being diluted by the Pfizer COVID-19 vaccine diluent, 2.2 mL of 0.9% sodium chloride (normal saline, preservative free) of the diluent used for Pfizer COVID-19 vaccine into the bottle of magenta border Moderna). At the time of the report, PRODUCT PREPARATION ERROR (The vaccine was administered after being diluted by the Pfizer COVID-19 vaccine diluent, 2.2 mL of 0.9% sodium chloride (normal saline, preservative free) of the diluent used for Pfizer COVID-19 vaccine into the bottle of magenta border Moderna) and UNDERDOSE (vaccine was administered, 0.2 mL dose and administered to 3 year 2 month child) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered PRODUCT PREPARATION ERROR (The vaccine was administered after being diluted by the Pfizer COVID-19 vaccine diluent, 2.2 mL of 0.9% sodium chloride (normal saline, preservative free) of the diluent used for Pfizer COVID-19 vaccine into the bottle of magenta border Moderna) and UNDERDOSE (vaccine was administered, 0.2 mL dose and administered to 3 year 2 month child) to be not related. No concomitant medications were reported. Patient age was reported as 3 years 2months. It was reported that the vaccine was administered to 2 children under the age of 4 years, The patients did not experience any side effects at that moment. The event did not caused patient to seek medical care. Patient had not experienced any similar event in the past. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 08-Jul-2022: The recent live follow-up received on 10-JUL-2022 contains fax number and narrative were updated. On 11-Jul-2022: Follow up received contains non significant information. On 18-Jul-2022: Follow up contains significant information: Additional reporter added. Patient demographics added. Suspect product details updated. Events details updated. I-narrative supplement updated. |
|
VAERS ID: |
2386928 (history) |
Form: |
Version 2.0 |
Age: |
4.0 |
Sex: |
Female |
Location: |
North Carolina |
Vaccinated: |
2022-07-15 |
Onset: |
2022-07-15 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
014B22A / 1 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: Patients received first dose 0.25ml from Red Cap adult vial; This spontaneous case was reported by an other health care professional and describes the occurrence of INCORRECT DOSE ADMINISTERED (Patients received first dose 0.25ml from Red Cap adult vial) in a 4-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 014B22A) for COVID-19 prophylaxis. No Medical History information was reported. On 15-Jul-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 15-Jul-2022, the patient experienced INCORRECT DOSE ADMINISTERED (Patients received first dose 0.25ml from Red Cap adult vial). At the time of the report, INCORRECT DOSE ADMINISTERED (Patients received first dose 0.25ml from Red Cap adult vial) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant drug was reported. The patient received Moderna COVID-19 vaccine from a vial with red cap and a label with light blue border. No Treatment medications were reported. This case was linked to MODERNATX, INC.-MOD-2022-609133 (E2B Linked Report).; Sender''s Comments: MODERNATX, INC.-MOD-2022-609133:CMOD22-03372- crosslink (2 year 11 months old patient), Same reporter |
|
VAERS ID: |
2386960 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Maryland |
Vaccinated: |
2022-07-18 |
Onset: |
2022-07-18 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1414B / 1 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Expired product administered, Product storage error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: Vial was first punctured on 15-Jul-2022 8.30 and dose adminisitered on 18-Jul-2022 9:30 am; Dose administered more than 12 hours post puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered more than 12 hours post puncture) and PRODUCT STORAGE ERROR (Vial was first punctured on 15-Jul-2022 8.30 and dose adminisitered on 18-Jul-2022 9:30 am) in a 2-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. AS1414B) for COVID-19 vaccination. No Medical History information was reported. On 18-Jul-2022 at 9:30 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Jul-2022 at 9:30 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered more than 12 hours post puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was first punctured on 15-Jul-2022 8.30 and dose adminisitered on 18-Jul-2022 9:30 am). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered more than 12 hours post puncture) and PRODUCT STORAGE ERROR (Vial was first punctured on 15-Jul-2022 8.30 and dose adminisitered on 18-Jul-2022 9:30 am) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Vial was initially stored in the refrigerator on 28-Jun-2022. Vial was first punctured on 15-Jul-2022 about 8:30 am. Post Puncture the vial was stored in Fridge. Vial did not undergo any temperature excursion. Total amount of time the vial was exposed to room temperature range (8 to 25 degree Celsius - 46 to 77 degree Fahrenheit) was unknown, but only taken out when a dose was to be drawn up. Probably less than an hour in total. Vial was exposed to room temperature for more that 24 hours. No treatment information was provided. |
|
VAERS ID: |
2387029 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Kansas |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
LL / OT |
Administered by: Unknown Purchased by: ? Symptoms: Accidental underdose, Incorrect dose administered, Product preparation error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: 2.2 mL of 0.9% sodium chloride (normal saline, preservative free) of the diluent used for Pfizer COVID-19 vaccine into the bottle of magenta border Moderna.; Vaccine with 0.2 mL dose was administered to a 2 years child; Vaccine with 0.2 mL dose was administered to 1 child that was 2 years; This spontaneous case was reported by a nurse and describes the occurrence of INCORRECT DOSE ADMINISTERED (Vaccine with 0.2 mL dose was administered to 1 child that was 2 years), PRODUCT PREPARATION ERROR (2.2 mL of 0.9% sodium chloride (normal saline, preservative free) of the diluent used for Pfizer COVID-19 vaccine into the bottle of magenta border Moderna.) and ACCIDENTAL UNDERDOSE (Vaccine with 0.2 mL dose was administered to a 2 years child) in a 2-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. AS1416B) for COVID-19 vaccination. No Medical History information was reported. On 08-Jul-2022 at 8:00 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .2 milliliter. On 08-Jul-2022 at 8:00 AM, the patient experienced INCORRECT DOSE ADMINISTERED (Vaccine with 0.2 mL dose was administered to 1 child that was 2 years) and ACCIDENTAL UNDERDOSE (Vaccine with 0.2 mL dose was administered to a 2 years child). On an unknown date, the patient experienced PRODUCT PREPARATION ERROR (2.2 mL of 0.9% sodium chloride (normal saline, preservative free) of the diluent used for Pfizer COVID-19 vaccine into the bottle of magenta border Moderna.). At the time of the report, INCORRECT DOSE ADMINISTERED (Vaccine with 0.2 mL dose was administered to 1 child that was 2 years), PRODUCT PREPARATION ERROR (2.2 mL of 0.9% sodium chloride (normal saline, preservative free) of the diluent used for Pfizer COVID-19 vaccine into the bottle of magenta border Moderna.) and ACCIDENTAL UNDERDOSE (Vaccine with 0.2 mL dose was administered to a 2 years child) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient race was reported. Patient was not diagnosed or tested positive with Covid-19. Concomitant medications details were not reported by the reporter. The vaccine was administered after being diluted by the Pfizer COVID-19 vaccine diluent, 2.2 mL of 0.9 percent sodium chloride (normal saline, preservative free) of the diluent used for Pfizer COVID-19 vaccine into the bottle of magenta border Moderna. No adverse reaction reported at the time of the report. Treatment details were not reported by the reporter. This case was linked to MOD-2022-610051 (Patient Link). |
|
VAERS ID: |
2387031 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Male |
Location: |
Kansas |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-13 |
Days after vaccination: |
5 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
AS1416B / 1 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Inappropriate schedule of product administration SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: First dose was administered on 08-Jul-22 and Second dose was administered on 13-Jul-22; This spontaneous case was reported by a nurse and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (First dose was administered on 08-Jul-22 and Second dose was administered on 13-Jul-22) in a 2-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. AS1416B) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Jul-2022 at 8:00 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .2 milliliter. On 13-Jul-2022 at 11:00 AM, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 13-Jul-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (First dose was administered on 08-Jul-22 and Second dose was administered on 13-Jul-22). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (First dose was administered on 08-Jul-22 and Second dose was administered on 13-Jul-22) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient was not diagnosed or tested positive with Covid-19. No concomitant medications were reported. No treatment medications were reported. No adverse event were at that time. This case was linked to MOD-2022-609975 (Patient Link). |
|
VAERS ID: |
2387046 (history) |
Form: |
Version 2.0 |
Age: |
1.58 |
Sex: |
Female |
Location: |
Arizona |
Vaccinated: |
2022-07-08 |
Onset: |
2022-07-08 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-23 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
017B22A / 1 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Accidental overdose, Off label use, Pain in extremity, Pyrexia, Somnolence SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Drug abuse and dependence (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Tendinopathies and ligament disorders (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20226 Write-up: sleeping more than usual; arm pain; fever; A 19 month old patient received their first dose of the Moderna COVID-19 vaccine by intramuscular injection on 8JUL2022 with lot number 017B22A, expiration date 14SEP2022, 0.5mL dose; A 19 month old patient received their first dose of the Moderna COVID-19 vaccine by intramuscular injection on 8JUL2022 with lot number 017B22A, expiration date 14SEP2022, 0.5mL dose; This spontaneous case was reported by an other health care professional and describes the occurrence of SOMNOLENCE (sleeping more than usual), PAIN IN EXTREMITY (arm pain), PYREXIA (fever), ACCIDENTAL OVERDOSE (A 19 month old patient received their first dose of the Moderna COVID-19 vaccine by intramuscular injection on 8JUL2022 with lot number 017B22A, expiration date 14SEP2022, 0.5mL dose) and OFF LABEL USE (A 19 month old patient received their first dose of the Moderna COVID-19 vaccine by intramuscular injection on 8JUL2022 with lot number 017B22A, expiration date 14SEP2022, 0.5mL dose) in a 19-month-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 017B22A) for COVID-19 vaccination. No Medical History information was reported. On 08-Jul-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 08-Jul-2022, the patient experienced SOMNOLENCE (sleeping more than usual), PAIN IN EXTREMITY (arm pain), PYREXIA (fever), ACCIDENTAL OVERDOSE (A 19 month old patient received their first dose of the Moderna COVID-19 vaccine by intramuscular injection on 8JUL2022 with lot number 017B22A, expiration date 14SEP2022, 0.5mL dose) and OFF LABEL USE (A 19 month old patient received their first dose of the Moderna COVID-19 vaccine by intramuscular injection on 8JUL2022 with lot number 017B22A, expiration date 14SEP2022, 0.5mL dose). The patient was treated with ACETAMINOPHEN ongoing since an unknown date for Fever, at an unspecified dose and frequency; IBUPROFEN ongoing since an unknown date for Fever, at an unspecified dose and frequency and ONDANSETRON at an unspecified dose and frequency. At the time of the report, SOMNOLENCE (sleeping more than usual), PAIN IN EXTREMITY (arm pain), PYREXIA (fever), ACCIDENTAL OVERDOSE (A 19 month old patient received their first dose of the Moderna COVID-19 vaccine by intramuscular injection on 8JUL2022 with lot number 017B22A, expiration date 14SEP2022, 0.5mL dose) and OFF LABEL USE (A 19 month old patient received their first dose of the Moderna COVID-19 vaccine by intramuscular injection on 8JUL2022 with lot number 017B22A, expiration date 14SEP2022, 0.5mL dose) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that this vaccine is not authorized for this population, but it was approved for use in people 12 years of age and older. |
|
VAERS ID: |
2387311 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Tennessee |
Vaccinated: |
2022-06-25 |
Onset: |
0000-00-00 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-24 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 1 |
- / - |
Administered by: Unknown Purchased by: ? Symptoms: Epistaxis SMQs:, Haemorrhage terms (excl laboratory terms) (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USPFIZER INC202200966777 Write-up: Severe nose bleed after both doses; approximately 12-15 hours after injection.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 3-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Jun2022 as dose 1, single (Batch/Lot number: unknown) at the age of 3 years, in left leg for covid-19 immunisation. The patient''s relevant medical history and concomitant medications were not reported. The following information was reported: EPISTAXIS (non-serious) with onset 2022, outcome "unknown", described as "Severe nose bleed after both doses; approximately 12-15 hours after injection.". Therapeutic measures were taken as a result of epistaxis. Additional information: Patient did not receive other vaccine in four weeks. Patient doesn''t have Covid-19 prior to vaccination and not been tested for Covid post vaccination. Patient had no known allergies. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received. |
|
VAERS ID: |
2387433 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Tennessee |
Vaccinated: |
2022-07-16 |
Onset: |
2022-07-17 |
Days after vaccination: |
1 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-24 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 2 |
LA / - |
Administered by: Pharmacy Purchased by: ? Symptoms: Epistaxis SMQs:, Haemorrhage terms (excl laboratory terms) (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USPFIZER INC202200968524 Write-up: Severe nose bleed after both doses; approximately 12-15 hours after injection.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 3-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Jul2022 at 11:15 as dose 2, single (Batch/Lot number: unknown) at the age of 3 years, in left arm for covid-19 immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: Unknown. Unable to locate or read the details, Location of injection: Leg Left), administration date: 25Jun2022, when the patient was 3-year-old, for COVID-19 Immunization, reaction(s): "Severe nose bleed after both doses; approximately 12-15 hours after injection". The following information was reported: EPISTAXIS (non-serious) with onset 17Jul2022, outcome "unknown", described as "Severe nose bleed after both doses; approximately 12-15 hours after injection.". Therapeutic measures were taken as a result of epistaxis. Additional information: Severe nose bleed after both doses; approximately 12-15 hours after injection. No other vaccine in four weeks. No vaccination prior covid. Not tested for covid post vaccination. No known allergies. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received. |
|
VAERS ID: |
2387816 (history) |
Form: |
Version 2.0 |
Age: |
2.0 |
Sex: |
Female |
Location: |
Maryland |
Vaccinated: |
2022-07-23 |
Onset: |
2022-07-23 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-24 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LG / IM |
Administered by: Other Purchased by: ? Symptoms: Product preparation error SMQs:, Medication errors (narrow) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Peds Pfizer vax given without diluting. Pt waited 15 min for monitoring with no reactions or symptoms of concern. Discharged with mother. |
|
VAERS ID: |
2387819 (history) |
Form: |
Version 2.0 |
Age: |
3.0 |
Sex: |
Female |
Location: |
Maryland |
Vaccinated: |
2022-07-23 |
Onset: |
2022-07-23 |
Days after vaccination: |
0 |
Submitted: |
0000-00-00 |
Entered: |
2022-07-24 |
Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FT9142 / 2 |
LA / IM |
Administered by: Other Purchased by: ? Symptoms: Product preparation issue SMQs:, Medication errors (broad) Life Threatening? No Birth Defect? No Died? No Permanent Disability? No Recovered? No Office Visit? No ER Visit? No ER or Doctor Visit? No Hospitalized? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: Write-up: Ped pfizer vaccine given to pt without diluting. Pt was monitored for 15 min with no signs, symptoms or issues. Discharged home with parents. |
|