You can download data related to medicines published on EMA's website in table format. The website automatically updates these data tables overnight.
To stay up-to-date with new and updated information on this website, see:
Find the following types of information on medicines in the table below:
All relevant information and documents on medicines authorised at a European Union (EU) level are available on medicine pages. This includes:
These pages also contain information on medicines for which the European Commission has refused a marketing authorisation, or has suspended or withdrawn the marketing authorisation after approval.
More up-to-date information on veterinary medicinal products is available on the Veterinary Medicines Information website.
For more information, see:
Find information on opinions on post-authorisation procedures and withdrawn applications in the table below.
Download post-authorisation procedures for medicines data tableDuring the post-authorisation stage of a medicine life-cycle, marketing authorisation holders can submit an application to change the terms of marketing authorisation. This is known as a variation.
At any stage of the assessment process, applicants can withdraw the application to EMA.
Information on approved post-authorisation procedures is available on medicine pages.
For more information, see:
Find information on all ongoing and completed referrals in the table below.
Download referrals data tableFor more information, see:
Find information on decisions related to paediatric investigation plans following evaluation from the Paediatric Committee (PDCO) in the table below.
Download paediatric investigation plans data tableFor more information, see:
Find information on the status of orphan designations following assessment from the Committee for Orphan Medicinal Products (COMP) in the table below.
Download orphan designations data tableFor more information, see:
Find information on the regulatory outcomes of periodic safety update report single assessments (PSUSAs) in the table below.
Download period safety update report single assessments data tableMarketing authorisation holders periodically submit PSURs following a medicine's authorisation. EMA and national competent authorities carry out a single joint assessment of all medicines containing the same active substance or combination of active substances to determine if there is a need to update marketing authorisations.
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Find information on direct healthcare professional communication (DHPCs) for human and veterinary medicines in the table below. These contain important new safety information about a medicine, including recommended actions that healthcare professionals should take.
Download direct healthcare professional communications data tableFind information on ongoing and resolved medicine supply shortages assessed by EMA in the table below. The table includes links to individual shortage notices that contain valuable information for healthcare professionals and patients, along with details on the availability of alternatives.
Download medicine supply shortages data tableFor each shortage, additional information about the situation in a specific country may be available from the national competent authority.
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Find information on the status and outcomes of assessments from EMA's Committee on Herbal Medicinal Products (HMPC) in the table below.
Download herbal medicines data tableFor more information, see:
Find information on the status of EMA's scientific opinions on high priority medicines for use outside of the EU in the table below.
Download medicines for use outside EU data tableFor more information, see: