This brand name is authorized in Austria, Canada, Estonia, Spain, Finland, Croatia, Ireland, Italy, Lithuania, Netherlands, Poland, Romania, United Kingdom, South Africa
The drug IVEMEND contains one active pharmaceutical ingredient (API):
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1
Fosaprepitant
UNII D35FM8T64X - FOSAPREPITANT DIMEGLUMINE
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Fosaprepitant is the prodrug of aprepitant and when administered intravenously is converted rapidly to aprepitant. The contribution of fosaprepitant to the overall antiemetic effect has not fully been characterised, but a transient contribution during the initial phase cannot be ruled out. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| IVEMEND Powder for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC code | Group title | Classification |
|---|---|---|
| A04AD12 | Aprepitant | A Alimentary tract and metabolism → A04 Antiemetics and antinauseants → A04A Antiemetics and antinauseants → A04AD Other antiemetics |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| Country: EE | Ravimiamet | Identifier(s): 1491397, 1491409 |
| Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 07437003 |
| Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 095813 |
| Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 184714 |
| Country: IT | Agenzia del Farmaco | Identifier(s): 041018019, 041018021, 041018033, 041018045 |
| Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1056405, 1056406 |
| Country: NL | Z-Index G-Standaard | Identifier(s): 15638227 |
| Country: NL | Z-Index G-Standaard, PRK | Identifier(s): 95230 |
| Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100239838 |
| Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W52761001, W52761002 |
| Country: ZA | Health Products Regulatory Authority | Identifier(s): 43/5.7.2/0001, 45/5.7.2/0871 |
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