Pharmacovigilance (PV) is defined by the World Health Organisation (WHO) as the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem.
Pharmacovigilance is therefore vital for the advancement of medical understanding, future research and product development. Any improvements in safety or understanding will ultimately lead to improvements in patient care.
Unipharm is responsible for collect and report suspected adverse reactions to the respective Supplier/Principal Company for their attention and assessment.
All queries and product related complaints are taken very seriously and treated with the strictest confidentiality.
As per Unipharm policy, all employees are required to report any issues relating to the safety or quality of Unipharm distributed medicines immediately. All spontaneous adverse events of distributed products are collected via email, letter, conversation or telephone call.
Phone: +974 44930058
How do I report an adverse reaction/PQC?
Alternatively, you can find appropriate form via below link and submit it.
The designated person will evaluate the data and will initiate the further course of actions.