Reporting suspected side effects to F. Hoffmann-La Roche Ltd

1. Your location

2. Please accept the disclaimer

F. Hoffmann-La Roche Ltd ("Roche") has legal obligations to record and/or report adverse events. Therefore, for such purposes your data will be processed in accordance with specific GVP (pharmacovigilance) legislation, as further described in the Roche Privacy Notice for Pharmacovigilance, medical information and product complaints.

Roche will keep a record of the personal data that you provide for the purpose of responding to your inquiry, to follow up on such requests, to maintain the information in the Roche global pharmacovigilance database, and to comply with our legal and regulatory recording and reporting obligations. The retention time of data is in accordance with respective laws and regulations.

By including personal data of another data subject in the form, you represent the lawfulness of processing of such personal data.

The Roche Privacy Policy provides further detailed information about your rights and how Roche processes personal data.

I acknowledge that my data is being processed as described above and in accordance with the Roche Privacy Policy & Privacy Notice for Pharmacovigilance, medical information and product complaints.

3. Select the product

To report a suspected side effect, please click on the relevant photograph of the Tamiflu product used below

  • Tamiflu Capsules

  • Tamiflu Suspension