ADVERSE EVENT REPORTING SYSTEM
Data Source Link: www.fda.gov
Serious report (Jan 2018 - Dec 2018)
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The below visual shows two dimensions i.e. Size & Colour. Size is the Total reports of adverse events (Death, Life-Threatening, Hospitalization, Disability, Congenital Anomaly, Required Intervention & Other Serious Report) whereas Colour is the percentage of serious reports amongst the total adverse events (Death, Life-Threatening, Disability & Other Serious Events)
PFIZER BRISTIOL AMGEN ENDO PHARMA NOVARTIS ABBVIE JANSSEN ROCHE MYLAN TEVA FDA-CTU CELGENE ASTRAZANECA GLAXOSMITHKLINE SANDOZ AUROBINDO GILEAD SCIENCES MERCK & CO BOEHRINGER INGELHEIM BAYER HEALTHCARE AVENTIS TAKEDA BIOGEN ASTELLAS ELI LILLY BAUSCH AND LOMB RANBAXY ACTELION OTSUKA ACORDA DAIICHI REGENERON UCB CIPLA APOTEX JAZZ MERCK SHARP LUPIN SHIRE BAXTER INCYTE UNITED THERAPEUTICS PHARMACYCLICS ALEXION CONCORDIA ALLERGAN WEST-WARD SANOFI AMAG FRESENIUS GLENMARK EISAI ALKERMES MACLEODS JOHNSON AND JOHNSON TESARO NOVO NORDISK DR REDDYS TORRENT PHARMA CSL BEHRING PURDUE SUNOVION ACADIA PHARMACEUTICALS CELLTRION LUNDBECK SAOL THERAPEUTICS VIIV IMPAX VIFOR ORION
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