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.

You can report suspected side effects to Teva using our online reporting form.

Go to form

_________________________

Teva Pharmacovigilance Privacy Policy

The information you provide in this form will be recorded by Teva as part of its pharmacovigilance obligations. This information may be shared with other Teva entities and national and European authorities to be evaluated and collated with other adverse events recorded about that product or active ingredient. Further information can be found in a more detailed Policy here.

• If you are not the subject of the report, whilst you do not need to obtain the patient’s consent to submit their information, you should direct the patient to this notice.
• If you are a healthcare professional, whilst you do not need to obtain the patient’s consent to submit their information, you should direct the patient to this notice.

For more information go to:

Pharmacovigilance Privacy Policy

_________________________

You can also report suspect side effect to Ireland's Health Products Regulatory Authority (HPRA) .

Go to HPRA website