Lexapro flat affect2/20/2024 The volume of ICSRs for a particular medicinal product may be influenced by many different factors, including but not limited to the extent of use of the product, publicity and the nature of the reactions. Thus, this database is only a repository of ICSRs provided for VigiBase, and shall not be considered as a systematic register of ADRs that have occurred or may occur. UMC is the WHO Collaborating Centre for International Drug Monitoring based in Uppsala, Sweden providing scientific leadership and operative support to the WHO Program for International Drug Monitoring ( The data contains reports of suspected ADRs, so called Individual Case Safety Reports (ICSRs), collected by national drug authorities in over 120 countries and span over more than 100 000 different medicinal products. This data is sourced from VigiBase, the World Health Organization’s (the “WHO”) global database for suspected adverse drug reactions “ADRs”, maintained by Uppsala Monitoring Centre (“UMC”). It is therefore not possible to calculate an incidence rate of these ADRs based on these data.Īdjustment disorder with depressed mood : 1ĭepersonalisation/derealisation disorder : 4 The number of reports shown does not necessarily reflect the actual change for an ADR to occur. One single report may refer to multiple ADRs For this reason, the number of reports may be higher than the number of reports shown in the overview. Since the aim of a voluntary reporting centre is to detect new adverse drug reactions, we ask healthcare professionals and consumers to report suspicions of ADRs, even if the causal relationship has not been proven. The fact that a possible side effect of a drug or vaccine is reported, does not imply that the reported symptoms are actually caused by the drug or vaccine. The selection that is shown is based on the ATC classification system of the World Health Organization. If you enter a brand name or generic name, all reports of products will be shown that contain the corresponding active substance. The reports shown on this website were received directly by the Netherlands Pharmacovigilance Centre Lareb. To ensure a correct interpretation of the results, the data shown may only be used for publications or other media after consulting Lareb.
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