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Furoxone

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Furoxone

Discontinued Warning IconPlease Note: This Brand Name drug is no longer available in the US.
(Generic versions may still be available.)

Furoxone Side Effects Center

Medical Editor: John P. Cunha, DO, FACOEP

Furoxone (furazolidone) is a synthetic antimicrobial nitrofuran used in the specific and symptomatic treatment of bacterial or protozoal diarrhea and enteritis caused by susceptible organisms. The brand name of this medication is discontinued, but generic versions may be available. Common side effects include lowered blood pressure, hives, fever, joint pain, rash, nausea, vomiting, or malaise.

The average adult dosage of Furoxone is one 100-mg tablet four times daily. Furoxone may interact with other drugs. Tell your doctor all medications and supplements you use. Tell your doctor if you are pregnant or plan to become pregnant before using Furoxone. Consult your doctor before breastfeeding.

Our Furoxone (furazolidone) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What is Prescribing information?

The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.

Furoxone FDA Prescribing Information: Side Effects
(Adverse Reactions)

SIDE EFFECTS

A few hypersensitivity reactions to Furoxone (furazolidone) have been reported including a fall in blood pressure, urticaria, fever, arthralgia, and a vesicular morbilliform rash. These reactions subsided following withdrawal of the drug. Nausea, emesis, headache, or malaise occur occasionally and may be minimized or eliminated by reduction in dosage or withdrawal of the drug.

Rarely, individuals receiving Furoxone (furazolidone) have exhibited an Antabuse® (disulfiram)-like reaction to alcohol characterized by flushing, slight temperature elevation, dyspnea, and in some instances, a sense of constriction within the chest. All symptomatology disappeared within 24 hours with no lasting ill effects. During nine years of clinical use and approximately 3.5 million courses of therapy (in the U. S. A. alone) in the published literature and documented case reports 43 cases have been reported † of which 14 were produced under experimental conditions with planned doses of the compound in excess of those recommended.

Three of these experienced a fall in blood pressure necessitating active therapy. Indications are that levarterenol (Levophed®) may be used to combat such hypotensive episodes since human studies show that this drug is not potentiated in patients treated with Furoxone (furazolidone) . (Indirectly acting pressor agents should be avoided.) The ingestion of alcohol in any form should be avoided during Furoxone (furazolidone) therapy and for four days thereafter to prevent this reaction.

Furoxone (furazolidone) may cause mild reversible intravascular hemolysis in certain ethnic groups of Mediterranean and Near-Eastern origin, and Negroes. This is due to an intrinsic defect of red blood cell metabolism in a small percentage of these ethnic groups, making them unusually susceptible to hemolysis by numerous compounds. It is necessary to observe such patients closely while receiving Furoxone (furazolidone) and to discontinue its use it there is any indication of hemolysis. Should not be administered to infants under 1 month of age because of the possibility of producing a hemolytic anemia due to immature enzyme systems (glutathione instability) in the early neonatal period.

Colitis, proctitis, anal pruritus, staphylococcic enteritis, renal or hepatic toxicity have not been a significant problem with Furoxone (furazolidone) .

Read the entire FDA prescribing information for Furoxone (Furazolidone) »

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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.


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