Ergocalciferol (ergocalciferol (vitamin D2))
Last reviewed · Source: First Databank (FDB) drug data
Overview
Ergocalciferol is a vitamin D analog.
USES: Vitamin D (ergocalciferol-D2, cholecalciferol-D3, alfacalcidol) is a fat-soluble vitamin that helps your body absorb calcium and phosphorus. Having the right amount of vitamin D, calcium, and phosphorus is important for building and keeping strong bones. Vitamin D is used to treat and prevent bone disorders (such as rickets, osteomalacia).
Vitamin D is made by the body when skin is exposed to sunlight. Sunscreen, protective clothing, limited exposure to sunlight, dark skin, and age may prevent getting enough vitamin D from the sun. Vitamin D with calcium is used to treat or prevent bone loss (osteoporosis).
Vitamin D is also used with other medications to treat low levels of calcium or phosphate caused by certain disorders (such as hypoparathyroidism, pseudohypoparathyroidism, familial hypophosphatemia). It may be used in kidney disease to keep calcium levels normal and allow normal bone growth. Vitamin D drops (or other supplements) are given to breastfed infants because breast milk usually has low levels of vitamin D.
Generic name: ergocalciferol (vitamin D2)
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
Today’s intelligence on Ergocalciferol
Indications
The following indications are listed for Ergocalciferol:
- Glucocorticoid-Induced Osteoporosis
- Hypocalcemia
- Hypoparathyroidism
- Osteomalacia
- Osteoporosis
- Prevention Of Vitamin D Deficiency
- Rickets
- Vitamin D Deficiency
- Vitamin D Dependent Rickets
- X-Linked Hypophosphatemic Osteomalacia
Also known as: Abnormally Decreased Serum Calcium, Active Rickets, Adult Rickets, Condition Due To Low Levels Of Pth, Familial Hypophosphatemia, Familial X-Linked Hypophosphatemic Vitamin D Refractory Rickets, Glucocorticoid Hormone-Induced Osteoporosis, Glucocorticoid Induced Osteoporosis, Glycocorticoid-Induced Osteoporosis, Late Rickets, Rachitis, Rachitis Tarda, Vitamin D Dependent Infantile Osteomalacia, Vitamin D Dependent Juvenile Osteomalacia, Vitamin D Dependent Rachitis, Vitamin D Resistant Rickets, Vitamin D-Resistant Osteomalacia, Vitamin D-Resistant Rickets.
Dosing
Each mg of ergocalciferol is equivalent to 40,000 USP units; each mcg of the drug is equivalent to 40 USP units.
Dosage is expressed by weight (mg, mcg) or in terms of units.
During therapy with ergocalciferol, dosage depends on the nature and severity of the patient's hypocalcemia and must be individualized to maintain serum calcium concentrations of 9-10 mg/dL. In patients with familial hypophosphatemia (vitamin D-resistant rickets) or hypoparathyroidism, determinations of serum calcium and phosphorus concentrations should be made every 2 weeks or more frequently as needed. In these patients, the manufacturers of ergocalciferol recommend that radiographic examination of the bones be performed every month until the condition stabilizes or is corrected; however, some clinicians believe that this is unnecessary.
The manufacturers state that patients with malabsorption syndrome should not receive oral ergocalciferol.
Ergocalciferol is usually administered orally once daily. Ergocalciferol has been administered IM+ in some patients (e.g., those with GI, liver, or biliary disease associated with malabsorption of vitamin D analogs); however, ergocalciferol injection is no longer commercially available in the US.
When ergocalciferol is administered as an oral solution, the oral syringe provided by the manufacturer should be used to measure the dose and administer the solution directly into the patient's mouth.
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Drug interactions
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There are no contraindication interactions for this drug.
There are no severe interactions for this drug.
There are no moderate interactions for this drug.
Contraindications
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There are no contraindication contraindications for this drug.
There are no severe contraindications for this drug.
There are no moderate contraindications for this drug.
Adverse reactions
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There are no severe adverse reactions for this drug.
There are no less severe adverse reactions for this drug.
Precautions
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ICD codes
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Formulary status
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Last reviewed · Source: First Databank (FDB) drug data
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