Report a Suspected Adverse Event

Adverse Event Reporting

An adverse event is any undesirable medical occurrence that arises after the use of a medicinal product, regardless of whether a causal relationship with the product has been established.

The information provided through this form contributes to the ongoing monitoring of the safety of our products and to the protection of patients and users.

Where can I find the lot number and expiry date?

They are usually printed on the outer packaging and on the product label. Illustrative image.

IGC-AD1 carton and bottle showing where to find the product name, lot number and expiry date

Adverse Event Details

Describe the event and, whenever possible, indicate its onset date, duration, severity, course, and outcome. Also specify whether the event has resolved, is ongoing, or required medical attention, hospitalization, discontinuation of the product, or another intervention.

Include any relevant medical history or clinical information from before, during, and after the event, as well as any other medications, products, or treatments used.

Patient Information

Reporter Information

Medical Information

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