Reporting Side Effects

Ensuring patient safety is extremely important to Teva and we take the safety of all our medicines seriously.

Teva continuously monitors the safety of all its medicinal products (both drugs and devices) by collecting information about any side effects patients experience. It is vital that the safety of all medicinal products is monitored throughout their marketed life - this is known as pharmacovigilance.

If a medicinal product causes a side effect, you can use the form below to let us know. The more we understand about the effects of our medicinal products, the more can be done to improve the safe use of our medicinal products.

We may contact you to find out more details about your report; however, we are unable to provide medical advice about your condition.

If you are concerned, in any way, about your treatment you should contact your healthcare professional.

Teva Pharmacovigilance Privacy Policy

The information you provide in this form will be recorded by Teva as part of its legal obligations related to our products and will be protected and handled confidentially and in line with applicable data protection laws and Teva’s Privacy Policy.

This information may be shared with other Teva entities and certain authorities to be evaluated and collated with other events (including quality) recorded about that product or active ingredient, in order to assess the benefit – risk balance of the medicines you have used and if needed to update the product information and for the purposes of attending to your request. The information you provide today may be stored outside the EU.

If you do not agree to these uses of your information and wish to object to these processing or wish to access, rectify or delete your personal information please inform our call handler or email EUPrivacy@tevaeu.com. Further information can be found in a more detailed notice here.

If you are not the subject of this report, please ensure that individual who is the subject of the report is aware of this submission, including the possible transmission of his/her personal information.

Teva Pharmacovigilance Privacy Policy

Did you contact Teva previously about this adverse event?*:
Did you report the event to the MHRA/HPRA:
Your Details:
About the Patient:
About the person who had the suspected side effect:
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Gender
Is the patient pregnant?
About the medicine(s) you think caused the suspected reaction:
* please complete this missing information
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Other medicines

Please tell us about any other medicines or remedies used at the time of having the suspected reaction(s).

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About the suspected reaction(s)
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* please complete this missing information
Please attach any documents including lab reports, medication history, patient history here.
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Please provide dates:
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Other information
Please attach any documents including lab reports, medication history, patient history here.
Accepted file formats: .doc, .docx
Add new file
Other questions

Please enter the name and address of your Doctor or GP surgery

* means the field is mandatory