Nephro-Fer Side Effects
Generic Name: ferrous fumarate
Note: This page contains side effects data for the generic drug ferrous fumarate. It is possible that some of the dosage forms included below may not apply to the brand name Nephro-Fer.
It is possible that some side effects of Nephro-Fer may not have been reported. These can be reported to the FDA here. Always consult a healthcare professional for medical advice.
For the Consumer
Applies to ferrous fumarate: chewable tablets, suspension
Other dosage forms:
Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Seek medical attention right away if any of these SEVERE side effects occur while taking ferrous fumarate (the active ingredient contained in Nephro-Fer)
Constipation; darkened or green stools; diarrhea; nausea; stomach upset.
Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black, tarry stools; blood or streaks of blood in the stool; fever; vomiting with continuing sharp stomach pain.
For Healthcare Professionals
Applies to ferrous fumarate: compounding powder, oral liquid, oral suspension, oral tablet, oral tablet chewable, oral tablet extended release
Gastrointestinal side effects are generally dose-related and have included nausea, constipation, anorexia, heartburn, vomiting and diarrhea. In addition, stools may appear darker in color in patients taking ferrous fumarate (the active ingredient contained in Nephro-Fer)
Oral preparations may rarely cause Hemoccult-positive stools, patients with positive tests generally require further work-up.
Gastrointestinal discomfort may be minimized by initiating ferrous fumarate therapy at smaller doses and gradually titrating upwards until the desired dose is achieved.
Gastrointestinal discomfort may also be minimized by administering each dose with food. However, concurrent administration of ferrous fumarate with food may decrease the amount of iron absorbed.
Constipation may be relieved by administering docusate sodium 100 mg to 200 mg per day in addition to increasing the intake of oral fluids, such as water.
It has been hypothesized that gastroenteritis is caused by bacteria that become virulent in the presence of iron overload resulting in a systemic infection. Treatment consists of discontinuing deferoxamine and initiating appropriate antimicrobial therapy.
Immunologic side effects have rarely included gastroenteritis associated with Yersinia enterocolitica and Listeria monocytogenes in patients with iron overload status receiving treatment with deferoxamine.
Local side effects have included gangrene.
Localized corrosion has been reported in a pregnant woman taking ferrous sulfate (tablet) that lodged in a Meckel's diverticulum.
There have also been reports of wax-matrix ferrous sulfate tablets (delayed-release) lodging in the bowels of patients with strictures.
Stained teeth have primarily occurred following ingestion of ferrous fumarate (the active ingredient contained in Nephro-Fer) liquid preparation. Liquid dosage forms should be diluted in juice or water and sipped through a straw to aid in prevention of staining.
Iron overload (i.e., hemosiderosis) has been reported in patients genetically predisposed, or have underlying disorders, that augment the absorption of iron. It has also occurred following administration of excessive parenteral iron therapy, combination of oral and parenteral iron, or in patients with hemoglobinopathies that were erroneously diagnosed as iron deficiency anemia. Hemosiderosis is treated with repeated phlebotomy or long-term administration of deferoxamine. The liver is particularly susceptible to toxicity in iron-overload states.
Other side effects have included stained teeth and iron overload (hemosiderosis). Secondary hemochromatosis due to prolonged iron ingestion has been reported rarely.
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