Medicinal products for human use

If you experience any side effects or adverse event, please talk to your doctor, nurse or pharmacist as soon as possible.

If you wish to report an adverse event to Krka please use the online form below.

You can also report adverse events to the Yellow Card Scheme.

Information on the person who reported the adverse reaction

Have you consulted a doctor, pharmacist or other healthcare professional about the adverse reaction, or has the patient done so?

On whose behalf are you reporting this adverse reaction?

Information on the person who experienced the adverse reaction



Information on the medicinal product that caused the adverse reaction

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Has the patient stopped taking the medicine?

Had the patient been taking any other medicine before the adverse reaction occurred?


Description of the adverse reaction and related information

Has the patient received a medicine for treating the adverse reaction?

Additional and legal information

May we contact you if we require additional information?

We would like to inform you that by reporting the adverse reaction you will be sending your personal information to Krka, d. d., Novo mesto, Slovenia. Krka is required to process and store such information in line with legislation on medicines. Your data will only be used for monitoring, analysing and reporting about product safety. Please find more details about personal data protection here.


Report on adverse reaction

Your report has been successfully recorded. You will receive a summary of the report on your email address.

Legal notice

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