Vitranol Fe 30 mg/1
Ferrous Fumarate, Folic Acid · TABLET · PureTek Corporation
Vitranol Fe is a tablet containing ferrous fumarate, folic acid at 30 mg/1, taken oral. Manufactured by PureTek Corporation.
Key Facts
- Brand Name
- Vitranol Fe
- Generic Name
- Ferrous Fumarate, Folic Acid
- NDC Code (Product)
59088-173- Manufacturer
- PureTek Corporation
- Strength
- 30 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Drug Class
- Vitamin C [EPC]; Vitamin D [EPC]
- Marketing Start
- 01/04/2021
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
INDICATIONS: Vitranol FE is indicated for the treatment of iron deficiency anemia and folate deficiency as in extended convalescence, menorrhagia, pregnancy, puberty, excessive blood loss, and advanced age. Also for treatment of condition in which iron deficiency and vitamin C deficiency occur together, along with a deficient intake or increased need for B-Complex vitamins in chronic and acute illness, as well as cases of metabolic stress, and in convalescence.
Dosage & Administration
DOSAGE AND ADMINISTRATION: Adults (persons over 12 years of age) One (1) Vitranol Fe Multivitamin caplet daily, between meals or as directed by a physician. Do not administer to children under the age of 12.
Warnings
WARNING: Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. Keep this product out of reach of children. In case of accidental overdose, call a doctor or poison control center immediately. Administration of folic acid alone is improper therapy for pernicious anemia and other megaloblastic anemias in which vitamin B 12 is deficient. Precaution Section Folic acid in doses above 0.1 mg daily may obscure pernicious anemia, in that hematologic remission can occur while neurological manifestations remain progressive. There is a potential danger in administering folic acid to patients with undiagnosed anemia, since folic acid may obscure the diagnosis of pernicious anemia by alleviating the hematologic manifestations of the disease while allowing the neurologic complications to progress. This may result in severe nervous system damage before the correct diagnosis is made. Adequate doses of vitamin B 12 may prevent, halt, or improve the neurologic changes caused by pernicious anemia. The patient’s medical conditions and consumption of other drugs, herbs, and/or supplements should be considered. For use on the order of a healthcare prac…
Contraindications
CONTRAINDICATIONS: This product is contraindicated in patients with known hypersensitivity to any of its ingredients; also, all iron compounds are contraindicated in patients with hemosiderosis, hemochromatosis, or hemolytic anemias. Pernicious anemia is a contraindication, as folic acid may obscure its signs and symptoms.
Drug Interactions
Drug Interactions: Vitranol FE is not recommended for and should not be given to patients receiving levodopa because the action of levodopa is antagonized by pyridoxine. There is a possibility of increased bleeding due to pyridoxine interaction with anticoagulants (e.g., Aspirin, Heparin, or Clopidogrel).
Adverse Reactions
Adverse Reactions: Folic Acid: Allergic sensitizations have been reported following both oral and parenteral administration of folic acid. Ferrous Fumarate: Gastrointestinal disturbances (anorexia, nausea, diarrhea, constipation) occur occasionally, but are usually mild and may subside with continuation of therapy. Although the absorption of iron is best when taken between meals, giving Vitranol FE after meals may control occasional gastrointestinal disturbances. Vitranol FE is best absorbed when taken at bedtime. Adverse reactions have been reported with specific vitamins and minerals but generally at levels substantially higher than those contained herein. However, allergic and idiosyncratic reactions are possible at lower levels. Iron, even at the usual recommended levels, has been associated with gastrointestinal intolerance in some patients.
Frequently Asked Questions
What is Vitranol Fe used for?
Vitranol Fe contains Ferrous Fumarate, Folic Acid. It is a tablet taken oral. Consult your doctor for specific uses.
Is Vitranol Fe a controlled substance?
Vitranol Fe is not classified as a controlled substance by the DEA.
What is the generic name for Vitranol Fe?
The generic name for Vitranol Fe is Ferrous Fumarate, Folic Acid. There are 11 other brand versions of Ferrous Fumarate, Folic Acid.
What is the NDC code for Vitranol Fe 30 mg/1?
The NDC (National Drug Code) for Vitranol Fe 30 mg/1 is 59088-173, listed by PureTek Corporation.