A Post Marketing Surveillance to Evaluate the Safety and Efficacy of Brilinta

Mise à jour : Il y a 4 ans
Référence : NCT01611272

Femme et Homme

Extrait

To identify the following items through the post marketing surveillance under routine clinical practice after marketing authorization of Brilinta Tablet: the occurrence of unrevealed Serious Adverse Events (SAEs), current status of occurrence of Adverse Events (AEs), the factors that may influence safety and efficacy of the drug.


Critère d'inclusion

  • Acute Coronary Syndromes

Liens