Individuals are urged to consult a professional to report suspected adverse drug reactions (ADRs) on their behalf.
If you are a distributor and would like to learn more about Pharmacovigilance and Suspected Adverse Drug Reactions,including your responsibilities, please request our training pack.
It is the reporter's responsibility to obtain the patient's authority if disclosing non-anonymised details. Any information provided will be used by the Alinter Group exclusively for the purposes of ADR monitoring. This may include sharing the information with national regulatory authorities in the UK, EEA and third countries. Submission of a Suspected Adverse Drug Reaction Report (ADR) form implies consent to the above.
Suspected Adverse Drug Reactions may reported using the following methods:
(Preferred Method)Access the form here .
EMAIL or FAX
Download our ADR report forms.
0844 357 9181
+44 844 357 9181 (if dialed outside the UK)
For help via email: contact us.