IVEMEND

This brand name is authorized in Austria, Canada, Estonia, Spain, Finland, Ireland, Lithuania, Netherlands, Poland, Romania, United Kingdom, South Africa

Active ingredients

The drug IVEMEND contains one active pharmaceutical ingredient (API):

1 Fosaprepitant
UNII D35FM8T64X - FOSAPREPITANT DIMEGLUMINE

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.

Read about Fosaprepitant

Medication package inserts

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

Medicine classification

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
Discover more medicines within A04AD12

Authorization and marketing

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: 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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