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FeRiva (Highly Soluble Oral Tablets): Side Effects, Uses, Dosage, Interactions, Warnings

FeRiva

Medical Author: John P. Cunha, DO, FACOEP Last updated on RxList: 1/10/2022

Drug Summary

What Is FeRiva?

FeRiva 21/7 (ascorbic acid, zinc glycinate, cyanocobalamin, ferrous asparto glycinate, folic acid, docusate sodium and succinic acid tablet) is a multivitamin/multimineral dietary supplement indicated for use in improving the nutritional status of patients with iron deficiency.

What Are Side Effects of FeRiva?

Common side effects of FeRiva 21/7 include:

  • allergic reactions

Dosage for FeRiva

The usual dosage of FeRiva 21/7 is one tablet daily with or without food or as prescribed by your healthcare provider. The FeRiva 21/7 Tablets blister pack supplies a 28-day course of iron therapy that consists of 21 red iron tablets and 7 purple placebo tablets. Take 1 red iron tablet daily for 21 days, followed by 1 purple placebo tablet daily for 7 days.

What Drugs, Substances, or Supplements Interact with FeRiva?

FeRiva may interact with other drugs. Tell your doctor all medications and supplements you use.

FeRiva During Pregnancy or Breastfeeding

Tell your doctor if you are pregnant or plan to become pregnant before using FeRiva 21/7. FeRiva 21/7 passes into breast milk. Consult your doctor before breastfeeding.

Additional Information

Our FeRiva 21/7 (ascorbic acid, zinc glycinate, cyanocobalamin, ferrous asparto glycinate, folic acid, docusate sodium and succinic acid tablet) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.

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.

Description for FeRiva

FeRiva 21/7™ tablets for oral administration is a 28-day iron supplement regimen that consists of 21 red, oval-shaped iron tablets and 7 purple, oval-shaped placebo tablets. Each red, oval-shaped iron tablet is debossed with “21” and “7” separated by line in the middle on the top-side of the tablet and blank on the other side. Each purple, oval shaped placebo tablet is blank on both sides of the tablet.

Uses for FeRiva

FeRiva 21/7® is a multivitamin/multimineral dietary supplement indicated for use in improving the nutritional status of patients with iron deficiency.

Dosage for FeRiva

Usual dosage is one tablet daily with or without food or as prescribed by your healthcare provider. The FeRiva 21/7® Tablets blister pack supplies a 28-day course of iron therapy that consists of 21 red iron tablets and 7 purple placebo tablets. Take 1 red iron tablet daily for 21 days, followed by 1 purple placebo tablet daily for 7 days. After 28 tablets have been taken a new course may be started if prescribed.

HOW SUPPLIED

FeRiva 21/7® tablets blister pack (75854-318-28) contains 21 red iron tablets and 7 purple placebo tablets. The listed product number is not a National Drug Code. Instead Avion Pharmaceuticals has assigned a product code formatted according to standard industry practice to meet the formatting requirements of pharmacy and health insurance computer systems.

Keep out of reach of children. Store between 20°- 25°C (68°- 77°F).

Avion Pharmaceuticals, LLC, Alpharetta, GA 30022. Revised: Dec 2019

Side Effects for FeRiva

Allergic sensitization has been reported following both oral and parenteral administration of folic acid.

Drug Interactions for FeRiva

No Information provided

Warnings for FeRiva

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.

Precautions for FeRiva

Folic acid alone is improper therapy in the treatment of pernicious anemia and other megaloblastic anemias where Vitamin B12 is deficient. Folic acid in doses above 1.0 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations progress. While prescribing this nutritional supplement for pregnant women, nursing mothers or for women prior to conception, their medical condition and other drugs, herbs and/or supplements consumption should be considered.

Overdose Information for FeRiva

No Information Provided

Contraindications for FeRiva

No Information Provided

Clinical Pharmacology for FeRiva

No Information Provided

Patient Information for FeRiva

No information provided. Please refer to the WARNINGS AND PRECAUTIONS sections.

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Report Problems to the Food and Drug Administration

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.