Suspected Adverse Drug Reactions

Individuals are urged to consult a medical 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.

To access our Online Suspected Adverse Drug Reaction Reporting Tool, please click the button below