BRINAVESS

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

Active ingredients

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

1 Vernakalant
UNII 7G4J1ZD9UQ - VERNAKALANT HYDROCHLORIDE

Vernakalant is an antiarrhythmic medicine that acts preferentially in the atria to prolong atrial refractoriness and to rate-dependently slow impulse conduction.

Read about Vernakalant

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
BRIVANESS 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
C01BG11 Vernakalant C Cardiovascular system → C01 Cardiac therapy → C01B Antiarrhythmics, class I and III → C01BG Other class I antiarrhythmics
Discover more medicines within C01BG11

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 02462400
Country: EE Ravimiamet Identifier(s): 1493423, 1493434
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 10645002
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 411305
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 372350
Country: HK Department of Health Drug Office Identifier(s): 61191
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8360, 8976
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1056397, 1056398
Country: NL Z-Index G-Standaard, PRK Identifier(s): 97640
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100236700
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W60089001, W60089002
Country: ZA Health Products Regulatory Authority Identifier(s): 45/6.2/0350, 45/6.2/0351

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