RESPREEZA

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, France, Ireland, Italy, Lithuania, Netherlands, Poland, Romania, Spain, UK.

Active ingredients

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

1
UNII F43I396OIS - .ALPHA.1-PROTEINASE INHIBITOR HUMAN
 

Human alpha1-proteinase inhibitor is understood to be the primary anti-protease in the lower respiratory tract, where it inhibits neutrophil elastase (NE). Normal healthy individuals produce sufficient alpha1-proteinase inhibitor to control the NE produced by activated neutrophils and are thus able to prevent inappropriate proteolysis of lung tissue by NE.

 
Read more about Alfa1 antitrypsin

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 RESPREEZA Powder and solvent for solution MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
B02AB02 Alfa1 antitrypsin B Blood and blood forming organs → B02 Antihemorrhagics → B02A Antifibrinolytics → B02AB Proteinase inhibitors
Discover more medicines within B02AB02

Authorization and marketing

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

Country Identification scheme Identifier(s)
EE Ravimiamet 1695045, 1789173, 1789184
ES Centro de información online de medicamentos de la AEMPS 1151006001, 1151006002, 1151006003
FR Base de données publique des médicaments 64642836, 65543887, 68323818
GB Medicines & Healthcare Products Regulatory Agency 346063
IT Agenzia del Farmaco 044479018, 044479020, 044479032
LT Valstybinė vaistų kontrolės tarnyba 1077846, 1086931, 1086932
NL Z-Index G-Standaard, PRK 129828, 167622, 167649
PL Rejestru Produktów Leczniczych 100354887, 100417872, 100417889
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W63059001

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