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  1. sideeffects.embl.deSIDER Side Effect Resource

    Side Effect Resource. SIDER contains information on marketed medicines and their recorded adverse drug reactions. The information is extracted from public documents and package inserts. The available information include side effect frequency, drug and side effect classifications as well as links to further information, for example drug–target ...

    • Drug list

      Click on the side effect counts or drug names to display...

    • Side Effects

      drug side effect resource. License: Except as otherwise...

    • Download

      Download - SIDER Side Effect Resource

    • About

      The SIDER Side Effect Resource represents an effort to...

  2. www.adrreports.eu › enEuropean database of suspected adverse drug reaction reports

    European database of suspected adverse drug reaction reports. Online access to suspected side-effect reports. On this website you can view data on suspected side-effects, also known as suspected adverse drug reactions, for authorised medicines in the European Economic Area (EEA).

  3. who-umc.org › vigibaseVigiBase | UMC

    VigiBase is the WHO global database of adverse event reports for medicines and vaccines. It is the largest database of its kind in the world, with over 35 million reports of suspected adverse effects of medicines submitted by member countries of the WHO PIDM since 1968.

  4. www.adrreports.eu › en › eudravigilanceEuropean database of suspected adverse drug reaction reports ...

    The system allows the detection of signals of suspected side effects that were previously unknown, and of new information on known side effects. Data collected in EudraVigilance. EudraVigilance Clinical Trials module: suspected unexpected serious adverse reactions (SUSARs) reported by sponsors of interventional clinical trials;

  5. www.ema.europa.eu › en › human-regulatory-overviewEudraVigilance | European Medicines Agency

    EudraVigilance is the system for managing and analysing information on suspected adverse reactions to medicines which have been authorised or being studied in clinical trials in the European Economic Area (EEA). The European Medicines Agency (EMA) operates the system on behalf of the European Union (EU) medicines regulatory network.