GIAPREZA

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

Active ingredients

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

1 Angiotensin II
UNII M089EFU921 - ANGIOTENSIN II

Angiotensin II raises blood pressure by vasoconstriction; increased aldosterone release via direct action of angiotensin II on the vessel wall is mediated by binding to the G-protein-coupled angiotensin II receptor type 1 on vascular smooth muscle cells which stimulates Ca2+/calmodulindependent phosphorylation of myosin and causes smooth muscle contraction.

Read about Angiotensin II

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
GIAPREZA Solution for injection FDA, National Drug Code (US) MPI, US: SPL/PLR
GIAPREZA 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
C01CX09 C Cardiovascular system → C01 Cardiac therapy → C01C Cardiac stimulants excl. cardiac glycosides → C01CX Other cardiac stimulants
Discover more medicines within C01CX09

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): 1800694, 1800706, 1849271
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 142069
Country: FR Base de données publique des médicaments Identifier(s): 64441114
Country: IT Agenzia del Farmaco Identifier(s): 048208019, 048208021, 048208033
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1088389, 1088390, 1092290
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100425067
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W69477001
Country: US FDA, National Drug Code Identifier(s): 68547-501

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