Report an adverse event AH

Medicinal products for veterinary use

Have you been using Krka medicines and have noticed an adverse reaction? Please let us know about it by filling in the following form.

Information on the sick animal or owner

Information on the person who reported the adverse reaction

Where did the adverse reaction occur?

Who experienced the adverse reaction?

an animal

a human

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Medicinal product

Medicinal products you suspect caused the adverse reaction

This image shows where you can locate the batch number:

I can’t find the batch number

Has the animal ever taken this medicine before?

yes

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Adverse reaction

Description of the adverse reaction and related information

Has the animal ever had a reaction to this medicine?

yes

If you wish you can even upload an image or a file with the description of the adverse reaction.

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Additional and legal information

May we contact you if we require additional information?

yes

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.

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Report on adverse reaction

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

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