Purefe Plus label

Purefe Plus

Purefe Plus Recall

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Side Effects & Adverse Reactions

Accidental overdose of Iron-containing products is the 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.


Folic acid alone is improper therapy in the treatment for pernicious anemia and other megaloblastic anemias where Vitamin B12 is deficient.

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

Uses

PureFe Plus 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 the treatment of conditions 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.

History

There is currently no drug history available for this drug.

Other Information

There are no additional details available for this product.

Purefe Plus Manufacturers

  • Purefe Plus | Puretek Corporation
    No Recall

    Purefe Plus | Puretek Corporation

    Purefe Plus | Puretek Corporation

    Adults (person over 12 years of age), one (1) capsule daily, orally, between meals, or as prescribed by a physician. Do not exceed recommended dosage. Do not administer to children under the age of 12.

    Call your doctor for medical advice about side effects. You may report suspected side effects to the FDA at 1-800-FDA-1088.