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 by clicking the button below:

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.

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