Adverse event reporting

In case you wish to report an adverse event, please fill the form below and send it to drugsafety@richter.hu or forward a print version to this address.

ADVERSE EVENT REPORTING FORM 

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Why should you report adverse events?

When a new medicine is introduced to the market, only information on the most common adverse events is available from clinical trials since the latter involve a limited number of patients and healthy subjects. Therefore, knowledge about less common adverse events is often scarce.

Adverse event reporting is necessary to gather more data about the safety aspects of new medicines when they are to be used in a wider population.
This data is collected via systematic work by healthcare professionals as well as manufacturers.
However, patients and medicine users can also contribute to improve drug safety.

How can I report an adverse event? 

Please download the reporting form below, complete and send via email, post or fax.

The form can be downloaded here:

ADVERSE EVENT REPORTING FORM