Contact for Medical Information, Reporting Safety and Quality Related Issues:

If you need more information about our products or wish to report an adverse event or product quality related issue, please contact our Medical Information department via email or telephone:

Phone: 0870 351 8960
medicalinformationuk@grunenthal.com

Adverse events should be reported:

If, as a patient, you get any side effects talk to your doctor, pharmacist or nurse.
This includes any possible side effects not listed in the package leaflet.
By reporting side effects you can help provide more information on the safety of this medicine. You can also report side effects directly via the Yellow Card scheme at https://yellowcard.mhra.gov.uk.
Adverse events should also be reported to Grunenthal Ltd., UK.

February 2021 M-ALL-UK-09-20-0001

Reporting adverse events (UK Healthcare Professionals):

Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/
Adverse events should also be reported to Grünenthal Limited
Please contact telephone 0800 254 5540 or medicalinformationuk@grunenthal.com

Reporting possible side effects (UK patients and general public):

Reporting of side effects: If you experience any side effects, talk to your doctor, pharmacist or nurse. This includes possible side effects not listed in the package leaflet. You can also report side effects directly via the Yellow Card Scheme at https://yellowcard.mhra.gov.uk/. Side effects should also be reported to Grünenthal Limited Medical Information on telephone 0800 254 5540 or medicalinformationuk@grunenthal.com. By reporting side effects, you can help provide more information on the safety of medicines.