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Drug Safety

Despite in-depth pre-clinical tests and clinical trials, and despite respecting strict regulatory manufacturing standards, side-effects can occur with medicines because patients can react differently to the disease and its treatment. We have well-established systems to closely monitor these adverse events and react rapidly to them.

Like other biopharmaceutical companies, UCB also receives adverse event reports every year concerning our drug products, which are reviewed internally and provided to the governing regulatory authorities. Our safety teams use various tools to identify potential safety issues that could be related to adverse events, which may or may not be associated with our medicines.

What to do if you experience side effects?

For patients: if you wish to report an adverse event related to one of our products please contact your healthcare provider. In addition, you can contact us using the webform available here

For healthcare professionals: if you wish to report an adverse event related to one of our products, please follow the current regulatory procedure in force in your country or you can contact us using the webform available here

Feel free to reach to us; should you have any safety concerns related to UCB products.

Drug Safety – India
Off No: 022-40491247 :
Fax No: 022- 40491199
Email: ds.ind@ucb.com