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European Veterinary Pharmacovigilance Reporting Form for MAHsSafety issues in animal sin humansLack of expected efficacyWithdrawal period issuesEnvironmental problemsSENDER Report identification CASE
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What is European Veterinary Pharmacovigilance Reporting for MAHs Form?

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European veterinary pharmacovigilance reporting is the process of monitoring and reporting adverse reactions or side effects of veterinary medicines in the European Union.
Marketing authorization holders of veterinary medicines in the European Union are required to file european veterinary pharmacovigilance reporting.
European veterinary pharmacovigilance reporting can be filled out online through the European Medicines Agency's website using the electronic submission system.
The purpose of european veterinary pharmacovigilance reporting is to ensure the safety and effectiveness of veterinary medicines by monitoring and analyzing adverse reactions or side effects.
The information that must be reported on european veterinary pharmacovigilance reporting includes details of the adverse reaction, the veterinary medicine involved, and any other relevant information.
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