Report adverse events
THIS SITE IS NOT INTENDED OR DESIGNED FOR REPORTING OF ADVERSE EVENTS
Roche is required to document reports of adverse events, both for comprehensive safety monitoring of its products and also to fulfill reporting requirements to Regulatory Authorities. It allows continued monitoring of the benefit/risk balance of the medicinal product.
An Adverse Event (AE), also known as a side effect, is an unwanted and unintended response in a patient, after receiving a medicinal product,that may or may not have been caused by treatment with this product. The information you provide helps to ensure the safety of our products and our patients. If you need to report an adverse event for one of Roche’s products please email us on pakistan.drug_safety@roche.com or report it online here
Please provide the brand name and batch number, where possible. It is very important that safety surveillance is carried out on a brand/product specific basis to ensure the information collected is accurate.
For Medical Information Query:
If you are healthcare professional and have question about one of Roche's products please contact us on the below email:
email to: Pakistan.medical_information@roche.com
▼ Additional monitoring:
Medicinal products which have an inverted black triangle next to their name in materials such as the Patient Information Leaflet are subject to additional monitoring. Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product.
M-PK-00001514
Date of preparation: January 2024