Dosing & Uses
Dosage Forms & Strengths
1 mcg = 40 international units (IU)
oral solution
- 8000IU/mL (200mcg/mL)
capsule
- 50,000IU (1.25mg)
tablet
- 400IU (10mcg)
- 2000IU (50mcg)
Nutritional Supplementation
Recommended daily allowance (RDA)
19-70 years: 600 IU (15 mcg)/day
Pregnant or lactating women: 600 IU (15 mcg)/day
Osteoporosis
Prophylaxis and treatment
>50 years: 800-1000 IU (20-25 mcg) PO once daily with calcium supplements
Hypoparathyroidism
50,000-200,000 IU (0.625-5 mg) PO once daily with calcium supplements
Vitamin D-Resistant Rickets
12,000-500,000 IU (0.3-12.5 mg) PO once daily
Familial Hypophosphatemia
10,000-60,000 IU (0.25-1.5 mg) PO once daily with phosphate supplements
Dosage Forms & Strengths
1 mcg = 40 IU
oral solution
- 8000IU/mL (200mcg/mL)
capsule
- 50,000IU (1.25mg)
tablet
- 400IU (10mcg)
- 2000IU (50mcg)
Nutritional Supplementation
RDA
0-12 months: 400 IU (10 mcg) PO once daily
1-18 years: 600 IU (15 mcg) PO once daily
Vitamin D-Resistant Rickets
12,000-500,000 IU (0.3-12.5 mg) PO once daily
Familial Hypophosphatemia
40,000-80,000 IU (1-2 mg) PO once daily with phosphate supplements; may be reduced after stage of growth is complete
Nutritional Supplementation
RDA
<70 years: 600 IU (15 mcg) PO once daily
>70 years: 800 IU (20 mcg) PO once daily
Interactions
Interaction Checker
No Results
Contraindicated
Serious - Use Alternative
Significant - Monitor Closely
Minor
Contraindicated (0)
Serious - Use Alternative (2)
- pexidartinib
vitamin D and pexidartinib both increase Other (see comment). Avoid or Use Alternate Drug. Pexidartinib can cause hepatotoxicity. Avoid coadministration of pexidartinib with other products know to cause hepatoxicity.
- pretomanid
vitamin D, pretomanid. Either increases toxicity of the other by Other (see comment). Avoid or Use Alternate Drug. Comment: Pretomanid regimen associated with hepatotoxicity. Avoid alcohol and hepatotoxic agents, including herbal supplements and drugs other than bedaquiline and linezolid.
Monitor Closely (25)
- aluminum hydroxide
vitamin D increases levels of aluminum hydroxide by Other (see comment). Use Caution/Monitor. Comment: Avoid coadministration. Chronic use of aluminum-containing antacids in conjunction with vitamin D can lead to aluminum retention and possible toxicity.
- calcium acetate
vitamin D, calcium acetate. Other (see comment). Use Caution/Monitor. Comment: The concurrent use of vitamin D with calcium salts is generally beneficial; in some patients this combination may result in hypercalcemia.
- calcium carbonate
vitamin D, calcium carbonate. Other (see comment). Use Caution/Monitor. Comment: The concurrent use of vitamin D with calcium salts is generally beneficial; in some patients this combination may result in hypercalcemia.
- calcium chloride
vitamin D, calcium chloride. Other (see comment). Use Caution/Monitor. Comment: The concurrent use of vitamin D with calcium salts is generally beneficial; in some patients this combination may result in hypercalcemia.
- calcium citrate
vitamin D, calcium citrate. Other (see comment). Use Caution/Monitor. Comment: The concurrent use of vitamin D with calcium salts is generally beneficial; in some patients this combination may result in hypercalcemia.
- calcium gluconate
vitamin D, calcium gluconate. Other (see comment). Use Caution/Monitor. Comment: The concurrent use of vitamin D with calcium salts is generally beneficial; in some patients this combination may result in hypercalcemia.
- chlorothiazide
chlorothiazide increases effects of vitamin D by Other (see comment). Use Caution/Monitor. Comment: Combination may increase hypercalcemic effect of vitamin D analogs. Use with caution.
- chlorthalidone
chlorthalidone increases effects of vitamin D by Other (see comment). Use Caution/Monitor. Comment: Combination may increase hypercalcemic effect of vitamin D analogs. Use with caution.
- cholestyramine
cholestyramine will decrease the level or effect of vitamin D by Other (see comment). Use Caution/Monitor. Bile acid sequestrants may decrease the absorption of fat-soluble vitamins. Administer vitamin supplementation at least 4 hours prior to cholestyramine.
- colesevelam
colesevelam will decrease the level or effect of vitamin D by Other (see comment). Use Caution/Monitor. Bile acid sequestrants may decrease the absorption of fat-soluble vitamins. Administer vitamin supplementation at least 4 hours prior to colesevelam.
- colestipol
colestipol will decrease the level or effect of vitamin D by Other (see comment). Use Caution/Monitor. Bile acid sequestrants may decrease the absorption of fat-soluble vitamins. Administer vitamin supplementation at least 4 hours prior to colestipol.
- digoxin
vitamin D increases toxicity of digoxin by Other (see comment). Use Caution/Monitor. Comment: Vitamin D may cause hypercalcemia which may affect the actions of digoxin and/or lead to cardiac arrhythmias.
- fosphenytoin
fosphenytoin decreases effects of vitamin D by Other (see comment). Use Caution/Monitor. Comment: Vitamin D supplementation or dosage adjustments may be required in patients who are receiving chronic treatment with anticonvulsants.
- hydrochlorothiazide
hydrochlorothiazide increases effects of vitamin D by Other (see comment). Use Caution/Monitor. Comment: Combination may increase hypercalcemic effect of vitamin D analogs. Use with caution.
- indapamide
indapamide increases effects of vitamin D by Other (see comment). Use Caution/Monitor. Comment: Combination may increase hypercalcemic effect of vitamin D analogs. Use with caution.
- magnesium citrate
vitamin D increases levels of magnesium citrate by Other (see comment). Use Caution/Monitor. Comment: Vitamin D can increase serum magnesium concentrations, particularly in the presence of renal impairment. The combined use of vitamin D and magnesium-containing products should be avoided, if possible, in patients with chronic renal failure.
- magnesium hydroxide
vitamin D increases levels of magnesium hydroxide by Other (see comment). Use Caution/Monitor. Comment: Vitamin D can increase serum magnesium concentrations, particularly in the presence of renal impairment. The combined use of vitamin D and magnesium-containing products should be avoided, if possible, in patients with chronic renal failure.
- methyclothiazide
methyclothiazide increases effects of vitamin D by Other (see comment). Use Caution/Monitor. Comment: Combination may increase hypercalcemic effect of vitamin D analogs. Use with caution.
- metolazone
metolazone increases effects of vitamin D by Other (see comment). Use Caution/Monitor. Comment: Combination may increase hypercalcemic effect of vitamin D analogs. Use with caution.
- mineral oil
mineral oil will decrease the level or effect of vitamin D by Other (see comment). Use Caution/Monitor. Avoid concomitant use of mineral oil and vitamin D supplements to avoid risk of decreased absorption of vitamin D. Applies to only oral administration of these agents.
- orlistat
orlistat will decrease the level or effect of vitamin D by Other (see comment). Use Caution/Monitor. When combination must be used, may consider administering vitamin D at least 2 hours before or after administration of orlistat.
- phenobarbital
phenobarbital decreases effects of vitamin D by Other (see comment). Use Caution/Monitor. Comment: Vitamin D supplementation or dosage adjustments may be required in patients who are receiving chronic treatment with anticonvulsants.
- phenytoin
phenytoin decreases effects of vitamin D by Other (see comment). Use Caution/Monitor. Comment: Vitamin D supplementation or dosage adjustments may be required in patients who are receiving chronic treatment with anticonvulsants.
- primidone
primidone decreases effects of vitamin D by Other (see comment). Use Caution/Monitor. Comment: Vitamin D supplementation or dosage adjustments may be required in patients who are receiving chronic treatment with anticonvulsants.
- sucralfate
vitamin D increases levels of sucralfate by Other (see comment). Use Caution/Monitor. Comment: Avoid coadministration. Vitamin D analogs may increase the absorption of aluminum from sucralfate. .
Minor (0)
Adverse Effects
Frequency Not Defined
Arrhythmias
Confusion
Constipation
Dry mouth
Headache
Hypercalcemia
Lethargy
Metallic taste
Muscle or bone pain
Nausea
Sluggishness
Vomiting
Warnings
Contraindications
Hypercalcemia
Hypervitaminosis D
Ergocalciferol (oral): Gastrointestinal (GI), liver, or biliary disease associated with malabsorption of vitamin D analogues
Documented hypersensitivity with drugs that could have allergenic crossreactivity with ergocalceferol
Cautions
Ergocalciferol: Use with caution in renal impairment (strong caution), heart disease, kidney stones, arteriosclerosis
Obtain serum calcium twice weekly during titration
Discontinue if patient becomes hypercalcemic
Presence of tartrazine in some products may cause allergic reactions
Vitamin D toxicity may last ≥2 months after therapy is discontinued
Restrict intake in infants with idiopathic hypercalcemia
Concurrent use of cardiac glycosides
Adequate clinical response to vitamin D therapy is dependent on adequate dietary calcium
Maintain normal serum phosphorous concentrations in patients treated for hyperphosphatemia to prevent metastatic calcification
When treating hypoparathyroidism, concomitant treatment with intravenous calcium, parathyroid hormone, and/or dihydrotachysterol may also be required
Adults with a body mass index (BMI) greater than 30 kg/m² are at high risk for vitamin D deficiency due to storage of vitamin D in adipose tissue; doses higher than recommended daily allowance may be required, but must be carefully monitored to avoid toxicity
Metabolism of vitamin D may be altered in patients with chronic kidney disease
In renal impairment, supplementation with ergocalciferol may be necessary; monitor closely
In patients with rickets, the range between therapeutic and toxic doses is narrow in vitamin D–resistant patients; adjust dose based on clinical response to avoid toxicity
Pregnancy & Lactation
Pregnancy category: C (ergocalciferol)
Lactation: Drug is distributed into breast milk; use with caution
Pregnancy Categories
A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.
B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk. C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done. D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk. X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist. NA: Information not available.Pharmacology
Mechanism of Action
Stimulates calcium and phosphate absorption from small intestine; stimulates phosphate resorption at renal tubule; stimulates secretion of calcium into blood from bone
Absorption
Peak effect: 1 month with daily dosing
Metabolism
Metabolized in liver
Elimination
Excretion: Urine
Images
BRAND | FORM. | UNIT PRICE | PILL IMAGE |
---|---|---|---|
Baby's Super Daily D3 oral
-
|
10 mcg/drop (400 unit/drop) drops | ||
D3-2000 oral
-
|
50 mcg (2,000 unit) capsule | ||
Replesta oral
-
|
1,250 mcg (50,000 unit) wafer | ||
Vitamin D3 oral
-
|
50 mcg (2,000 unit) tablet | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) tablet | ||
Vitamin D3 oral
-
|
50 mcg (2,000 unit) capsule | ||
Vitamin D3 oral
-
|
50 mcg (2,000 unit) capsule | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) capsule | ||
Vitamin D3 oral
-
|
10 mcg (400 unit) capsule | ||
Vitamin D3 oral
-
|
10 mcg (400 unit) tablet | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) chewable tablet | ||
Vitamin D3 oral
-
|
50 mcg (2,000 unit) capsule | ||
Vitamin D3 oral
-
|
50 mcg (2,000 unit) tablet | ||
Vitamin D3 oral
-
|
10 mcg (400 unit) capsule | ||
Vitamin D3 oral
-
|
10 mcg (400 unit) tablet | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) tablet | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) capsule | ||
Vitamin D3 oral
-
|
50 mcg (2,000 unit) tablet | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) tablet | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) tablet | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) chewable tablet | ||
Vitamin D3 oral
-
|
10 mcg (400 unit) tablet | ||
Vitamin D3 oral
-
|
10 mcg (400 unit) tablet | ||
Vitamin D3 oral
-
|
50 mcg (2,000 unit) capsule | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) capsule | ||
Vitamin D3 oral
-
|
125 mcg (5,000 unit) tablet | ||
Vitamin D3 oral
-
|
50 mcg (2,000 unit) tablet | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) chewable tablet | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) chewable tablet | ||
Vitamin D3 oral
-
|
25 mcg (1,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
1,250 mcg (50,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
1,250 mcg (50,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
50 mcg (2,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
250 mcg (10,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
50 mcg (2,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
250 mcg (10,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
250 mcg (10,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
10 mcg/drop (400 unit/drop) drops | ||
cholecalciferol (vitamin D3) oral
-
|
10 mcg/mL (400 unit/mL) drops | ||
cholecalciferol (vitamin D3) oral
-
|
1,250 mcg (50,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
250 mcg (10,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
50 mcg (2,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
250 mcg (10,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
50 mcg (2,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
50 mcg (2,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
250 mcg (10,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
10 mcg/mL (400 unit/mL) drops | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
50 mcg (2,000 unit) chewable tablet | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) chewable tablet | ||
cholecalciferol (vitamin D3) oral
-
|
50 mcg (2,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
50 mcg (2,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) chewable tablet | ||
cholecalciferol (vitamin D3) oral
-
|
50 mcg (2,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) chewable tablet | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) chewable tablet | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
250 mcg (10,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
10 mcg/mL (400 unit/mL) drops | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
1,250 mcg (50,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
125 mcg (5,000 unit) capsule | ||
cholecalciferol (vitamin D3) oral
-
|
50 mcg (2,000 unit) tablet | ||
cholecalciferol (vitamin D3) oral
-
|
25 mcg (1,000 unit) tablet | ||
Dialyvite Vitamin D3 Max oral
-
|
1,250 mcg (50,000 unit) tablet | ||
D-Vi-Sol oral
-
|
10 mcg/mL (400 unit/mL) drops | ||
Decara oral
-
|
625 mcg (25,000 unit) capsule | ||
Decara oral
-
|
625 mcg (25,000 unit) capsule | ||
Decara oral
-
|
1,250 mcg (50,000 unit) capsule | ||
Decara oral
-
|
1,250 mcg (50,000 unit) capsule | ||
Decara oral
-
|
1,250 mcg (50,000 unit) capsule | ||
Thera-D oral
-
|
50 mcg (2,000 unit) tablet | ||
Thera-D 4000 oral
-
|
100 mcg (4,000 unit) tablet | ||
Super Daily D3 oral
-
|
25 mcg/drop ( 1000 unit/drop) drops | ||
Replesta NX oral
-
|
350 mcg (14,000 unit) wafer |
Copyright © 2010 First DataBank, Inc.
Patient Handout
cholecalciferol (vitamin D3) sublingual
NO MONOGRAPH AVAILABLE AT THIS TIME
USES: Consult your pharmacist.
HOW TO USE: Consult your pharmacist.
SIDE EFFECTS: Consult your pharmacist.In the US -Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www.fda.gov/medwatch.In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.
PRECAUTIONS: Consult your pharmacist.
DRUG INTERACTIONS: Consult your pharmacist.Keep a list of all your medications with you, and share the list with your doctor and pharmacist.
OVERDOSE: If someone has overdosed and has serious symptoms such as passing out or trouble breathing, call 911. Otherwise, call a poison control center right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center.
NOTES: No monograph available at this time.
MISSED DOSE: Consult your pharmacist.
STORAGE: Consult your pharmacist.Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.
Information last revised July 2016. Copyright(c) 2024 First Databank, Inc.
IMPORTANT: HOW TO USE THIS INFORMATION: This is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate for you. This information is not individual medical advice and does not substitute for the advice of your health care professional. Always ask your health care professional for complete information about this product and your specific health needs.
Formulary
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