| Clinical data | |
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| Trade names | Monoferric, Monofer |
| AHFS/Drugs.com | Monograph |
| License data | |
| Routes of administration | Intravenous (IV) |
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| Legal status | |
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| Identifiers | |
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| CAS Number | |
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| Chemical and physical data | |
| Formula | C18H34FeO16+3 |
| Molar mass | 562.299 g·mol−1 |
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Ferric derisomaltose (FDI), sold under the brand name Monoferric among others, is a medication for the treatment of iron deficiency anemia (IDA) in adults who have intolerance to oral iron or have had unsatisfactory response to oral iron or who have non-hemodialysis dependent chronic kidney disease (NDD-CKD).[3] It was approved for use in the United States in January 2020.[3][4][5] It is given intravenously.[3]
References
- ↑ "Monofer iron (as ferric derisomaltose) 1000 mg/10 mL solution for injection vial (290834)". Therapeutic Goods Administration (TGA). 26 May 2022. Retrieved 9 April 2023.
- ↑ "Search Page - Drug and Health Product Register". 23 October 2014.
- 1 2 3 4 "Monoferric- ferric derisomaltose solution". DailyMed. 24 January 2020. Retrieved 16 February 2020.
- ↑ "Monoferric approval letter" (PDF). U.S. Food and Drug Administration (FDA). 16 January 2020. Retrieved 16 February 2020.
This article incorporates text from this source, which is in the public domain. - ↑ "Drug Approval Package: Monoferric Injection". U.S. Food and Drug Administration (FDA). 7 May 2020. Retrieved 13 August 2020.
External links
- "Ferric derisomaltose". Drug Information Portal. U.S. National Library of Medicine.
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