FETCROJA

This brand name is authorized in Austria, Estonia, Spain, France, Croatia, Ireland, Italy, Lithuania, Poland, Romania, United Kingdom

Active ingredients

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

1 Cefiderocol
UNII TTP8LBP45D - CEFIDEROCOL SULFATE TOSYLATE

Cefiderocol is a siderophore cephalosporin. In addition to passive diffusion through outer membrane porin channels, cefiderocol is able to bind to extracellular free iron via its siderophore side chain, allowing active transport into the periplasmic space of Gram-negative bacteria through siderophore uptake systems. Cefiderocol subsequently binds to penicillin binding proteins (PBPs), inhibiting bacterial peptidoglycan cell wall synthesis which leads to cell lysis and death.

Read about Cefiderocol

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
FETCROJA Powder for concentrate 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
J01DI04 J Antiinfectives for systemic use → J01 Antibacterials for systemic use → J01D Other beta-lactam antibacterials → J01DI Other cephalosporins
Discover more medicines within J01DI04

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): 1818457
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1201434
Country: FR Base de données publique des médicaments Identifier(s): 64450362
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 387060
Country: IT Agenzia del Farmaco Identifier(s): 048722019
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1090105
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100441988
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W70044001

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