Ferrous Fumarate
Iron Bivalent, Oral Preparations
Sold as Integra F
- Drug class
- Iron Bivalent, Oral Preparations
- Availability
- Prescription only
- Routes
- Oral
- Markets covered
- 2
- Products on record
- 7
- FDA reports (12 mo)
- 331
Overview
Plain-language summary, compiled from the cited regulatory records
Ferrous fumarate is an iron supplement used to treat iron deficiency anemia and folate deficiency anemia [1]. It belongs to the drug class of oral iron bivalent preparations [1].
Ferrous fumarate is approved for use during pregnancy to prevent and treat iron deficiency and to provide a maintenance dosage of folic acid [1]. This active ingredient is available under various brand names, including Integra F [1].
In the past 12 months, there have been 331 adverse event reports associated with ferrous fumarate [2]. The most frequently reported issues include off-label use, nausea, product dose omission, the drug being ineffective, and fatigue [2].
This is not medical advice. Consult a qualified healthcare professional.
Regulatory status by market
| Market | Regulator | Products | Last revision |
|---|---|---|---|
| GB United Kingdom | MHRA | 6 | May 22, 2026 |
| US United States | FDA | 1 | November 8, 2022 |
GBUnited Kingdom· MHRA
6 products
Uses
Prophylaxis and treatment of iron deficiency states. For prophylaxis during pregnancy, a combination of iron and folic acid is usually recommended.
How to take
USUnited States· FDA
1 product
Uses
INDICATIONS:
Integra FTM is indicated for the treatment of iron deficiency anemia, and folate deficiency anemia. Integra FTM is indicated in pregnancy for the prevention and treatment of iron deficiency and to supply a maintenance dosage of folic acid.
How to take
Drug interactions
Known interactions involving Ferrous Fumarate. Select one for details. This list is informational and not a complete interaction checker.
Interaction data compiled from DDInter (academic, CC-BY). Severity classification only - this is not a complete interaction checker and not medical advice.
Sources & citations
- [1]MHRA (UK) · PL127620226 · revised April 10, 2026
- [2]FDA DailyMed · 025fee85-53a8-41… · revised November 8, 2022 [PDF]
- [3]OpenFDA adverse-event reports (US), 12 months ending June 4, 2026.
Information on this page is compiled from public regulatory records. Drugvu is not affiliated with any regulator or pharmaceutical manufacturer. This is not medical advice. Always consult a qualified healthcare professional.