Reporting makes medicines safer.
Timely reporting of safety information linked to our medicines plays a vital role in safer use and better patient outcomes.
We are steadfast in improving patient care and safety by embracing Good Pharmacovigilance Practices. Our objective is to encourage and facilitate reporting of suspected adverse effects related to Medisure products, to us and to the national authorities, by healthcare professionals, patients, parents and carers.
It is our moral and professional responsibility to keep working for patient safety with both our older and newer products.
We receive suspected adverse events for Medisure products only. All personal information related to adverse event reporting is processed in accordance with data protection legislation.
What to report
Report any adverse event after taking a Medisure product, even if you are unsure the medicine caused it. Serious and non-serious events both count. Highlighted items are serious.
Questions about drug safety
No questions match. Call +92-(0)312-2111164 and our team will help.
What is Medisure Drug Safety?
A Medisure Drug Safety (pharmacovigilance) programme for the collection, detection, assessment, monitoring and prevention of adverse events from Medisure medicinal products once they are authorised for patients' use.
It encourages reporting of suspected adverse events related to any of our products, including unwanted effects or unknown benefits, and builds trust in the overall safety and efficacy of Medisure products.
Report a suspected adverse event
Fields marked * are required. We cannot give medical advice: if your symptoms worry you or get worse, contact your doctor.