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Link to EudraVigilance: where can I find information on other reports made by patients?
Since April 2012, the European Medicines Agency has opened one of its “treasure chests” to the public: all reports made by patients, consumers, healthcare professionals, and industry are collected and stored in a database called EudraVigilance. This database contains millions of suspected adverse drug reactions and other information, which before April 2012, only pharmacovigilance experts and the pharmaceutical industry could access.
If you connect on the Internet to www.adrreports.eu, you can access information extracted from the EudraVigilance database. You can search for a specific medicine and access the information that can be publicly released on any suspected reactions reported for that medicine.
The European Database of Suspected Adverse Drug Reactions Reports http://www.adrreports.eu |
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The voice of rare disease patients in Europe
The international voice of people living with rare diseases
Bringing together patients, families and experts to share experiences in a moderated multi-language forum.
The Rare Barometer Programme is a EURORDIS initiative that carries out surveys to transform rare disease patients' experiences into figures and facts that can be shared with decision-makers.
An international awareness raising campaign taking place on the last day of February each year, Rare Disease Day is a EURORDIS initiative
Join the largest gathering of rare disease stakeholders across Europe, at the biennial European Conference on Rare Diseases and Orphan Products. ECRD is a EURORDIS initiative
The international voice of people living with rare diseases
Bringing together patients, families and experts to share experiences in a moderated multi-language forum.
The Rare Barometer Programme is a EURORDIS initiative that carries out surveys to transform rare disease patients' experiences into figures and facts that can be shared with decision-makers.
An international awareness raising campaign taking place on the last day of February each year, Rare Disease Day is a EURORDIS initiative
Join the largest gathering of rare disease stakeholders across Europe, at the biennial European Conference on Rare Diseases and Orphan Products. ECRD is a EURORDIS initiative