pharmacopeia

Vitamin D3

US-FDASourced from openFDA
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Indications

Sourced from openFDA
  • Folixate ™ is indicated for dietary management of patients with unique nutritional needs requiring increased folate level and Vitamin D supplementation. Folixate™ can be taken by women of childbearing age, pregnant women, and lactating and nonlactating mothers.

Contraindications

Sourced from openFDA
  • This product is contraindicated in patients with a known hypersensitivity to any of the ingredients. Folixate ™ is contraindicated in patients with hypercalcemia, malabsorption syndrome, abnormal sensitivity to the toxic effects of Vitamin D, and hypervitaminosis D.contraindicated

Dosage & administration

Sourced from openFDA

Take one tablet daily or as directed by a licensed healthcare practitioner.

Warnings & precautions

Sourced from openFDA

Tell your doctor if you have: kidney problems, thyroid disease. This medication should be used as directed during pregnancy or while breast-feeding. Consult your doctor about the risks and benefits. Folate alone is improper therapy in the treatment of pernicious anemia and other megaloblastic anemias where Vitamin B12 is deficient. Folate in doses above 0.1 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations progress.

Adverse reactions

Sourced from openFDA

Allergic sensitization has been reported following both oral and parenteral administration of folate. You should call your doctor for medical advice about serious adverse events. To report adverse side effects or to obtain product information, contact PureTek Corporation, at 1-877-921-7873.

FAERS reports

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Reference statistics only. FAERS reports are voluntarily submitted and are not incidence rates, safety signals, or causal evidence. Counts reflect reporting volume — how often a reaction was reported, not how often it occurs. For decision-grade use, consult openFDA and the FAERS Public Dashboard directly.
223 total reports matchedLatest report Share = reports listing the reaction ÷ total matched reports. Rows can sum to >100% because a single report often lists multiple reactions.
  1. 1Nausea3415%
  2. 2Dyspnoea219.4%
  3. 3Diarrhoea188.1%
  4. 4Abdominal Pain177.6%
  5. 5Asthenia167.2%
  6. 6Dizziness167.2%
  7. 7Fatigue167.2%
  8. 8Haemoglobin Decreased156.7%
  9. 9Headache156.7%
  10. 10Pneumonia156.7%
  11. 11Vomiting146.3%
  12. 12Arthralgia125.4%
  13. 13Fall125.4%
  14. 14Anaemia104.5%
  15. 15Malaise104.5%

Literature

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Recent PubMed references pinned to Vitamin D3 as a MeSH major topic. Citations link to pubmed.ncbi.nlm.nih.gov.

Clinical trials

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The 10 most recently updated of 3,256 ClinicalTrials.gov registrations naming Vitamin D3 as an intervention. Registration is not evidence of efficacy or safety — reference crosswalk only.

Frequently asked questions

What is Vitamin D3 used for?
According to FDA labeling, Vitamin D3 carries indications including: Folixate ™ is indicated for dietary management of patients with unique nutritional needs requiring increased folate level and Vitamin D supplementation. Folixate™ can be taken by women of childbearing age, pregnant women, and lactating and nonlactating mothers.. This is a reference summary of labeled uses, not medical advice or a treatment recommendation.
What are the contraindications for Vitamin D3?
Vitamin D3 labeling lists contraindications including: This product is contraindicated in patients with a known hypersensitivity to any of the ingredients. Folixate ™ is contraindicated in patients with hypercalcemia, malabsorption syndrome, abnormal sensitivity to the toxic effects of Vitamin D, and hypervitaminosis D.. Always consult the full prescribing information and a clinician.
Note. Data for vitamin-d3 is illustrative MVP content compiled from public sources. pharmacopeia is for educational and informational use only and is not a substitute for professional medical advice.

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