IKERVIS

This brand name is authorized in Austria, Cyprus, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Italy, Lithuania, Netherlands, Poland, Romania, Singapore, United Kingdom

Active ingredients

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

1 Ciclosporin
UNII 83HN0GTJ6D - CYCLOSPORINE

Ciclosporin (also known as ciclosporin A) is a cyclic polypeptide immunomodulator with immunosuppressant properties. It has been shown to prolong survival of allogeneic transplants in animals and significantly improved graft survival in all types of solid organ transplantation in man. Ciclosporin has also been shown to have an anti-inflammatory effect.

Read about Ciclosporin

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
IKERVIS Eye drops, emulsion 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
S01XA18 Ciclosporin S Sensory organs → S01 Ophthalmologicals → S01X Other ophthalmologicals → S01XA Other ophthalmologicals
Discover more medicines within S01XA18

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): 1683097, 1683109
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 115990001
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 392390
Country: FR Base de données publique des médicaments Identifier(s): 65881230
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 299509
Country: HK Department of Health Drug Office Identifier(s): 65076
Country: IE Health Products Regulatory Authority Identifier(s): 30735
Country: IT Agenzia del Farmaco Identifier(s): 044013011, 044013023, 044013035, 044013047, 044013050
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1076105, 1076106
Country: NL Z-Index G-Standaard, PRK Identifier(s): 196452
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100342542
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W62621001, W62621002
Country: SG Health Sciences Authority Identifier(s): 15216P

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