RAPORT DE REACŢIE ADVERSĂ SUSPECTATĂ

Sun Pharma are un angajament puternic pentru fabicarea produselor de calitate, O baza de date corespunzătoare de raportare a evenimentelor adverse este menţinută pentru a se asigura că reglementările de conformitate sunt respectate la nivel global. Va rugăm să ne ajutaţi completând formularul de mai jos în cazul unei reacţii adverse. Informaţiile generate bazate pe aceste rapoarte ajută la evaluarea continuă a raportului beneficiu-risc al medicamentelor.

Ce trebuie raportat?

• Customers, Healthcare Professionals can report ‘Any Adverse Experience / Side Effect’ experienced after taking Sun Pharma medicine(s).
• Besides, these are other scenarios/ situations (cited below as examples) which can be reported to Sun Pharma, Pharmacovigilance department for any SunPharma drug that is in question
• Patient taking company drug  was pregnant → Report to Pharmacovigilance department as pregnancy
• Company drug on patient X didn’t work → Report to Pharmacovigilance department as Lack of efficacy
• Patient has overdosed on product X (Company drug) → Report to Pharmacovigilance department as overdose
• Pack of Company  tablets that are discoloured, or damaged → Report as Product Complaint
• Patients reports that their tablet was a funny shape → Report as Product Complaint
• Adverse Event is already identified within the label – would you still report this? → Report everything to Pharmacovigilance department
• What if an AE is reported to you as the company representative, but no trade name is given → Report everything to Pharmacovigilance department
  

Cine poate raporta:

Orice profesionist din domeniul sănătății (medici, stomatologi, asistente medicale, farmaciști, pacienți etc.)
Non-profesional din domeniul sănătății (pacient, rudă, prieten etc.)