This brand name is authorized in Canada, Cyprus, Spain, Finland, France, Ireland, Malta, New Zealand, Poland, United Kingdom, United States
The drug RIASTAP contains one active pharmaceutical ingredient (API):
1
Human fibrinogen
UNII N94833051K - FIBRINOGEN HUMAN
|
Human fibrinogen (coagulation factor I), in the presence of thrombin, activated coagulation factor XIII (F XIIIa) and calcium ions is converted into a stable and elastic three-dimensional fibrin haemostatic clot. The administration of human fibrinogen concentrate provides an increase in plasma fibrinogen level and can temporarily correct the coagulation defect of patients with fibrinogen deficiency. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
RIASTAP Powder for solution for injection or infusion | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
B02BB01 | Human fibrinogen | B Blood and blood forming organs → B02 Antihemorrhagics → B02B Vitamin K and other hemostatics → B02BB Fibrinogen |
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): 02393352 |
Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 72725 |
Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 422474 |
Country: FR | Base de données publique des médicaments | Identifier(s): 61179660 |
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 185608 |
Country: MT | Medicines Authority | Identifier(s): MA665/00401 |
Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 18613 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100244762 |
Country: US | FDA, National Drug Code | Identifier(s): 63833-891 |
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