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10.1146/annurev-pharmtox-011613-135955

http://scihub22266oqcxt.onion/10.1146/annurev-pharmtox-011613-135955
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C4677571!4677571!25292435
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suck abstract from ncbi


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pmid25292435      Annu+Rev+Pharmacol+Toxicol 2015 ; 55 (ä): 75-87
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  • Improving Post-Approval Drug Safety Surveillance: Getting Better Information Sooner #MMPMID25292435
  • Hennessy S; Strom BL
  • Annu Rev Pharmacol Toxicol 2015[]; 55 (ä): 75-87 PMID25292435show ga
  • Adverse drug events (ADEs) are an important public health concern, accounting for 5% of all hospital admissions and two-thirds of all complications occurring shortly after hospital discharge. There are often long delays between when a drug is approved and when serious ADEs are identified. Recent and ongoing advances in drug safety surveillance include establishment of government-sponsored networks of population databases, use of data mining approaches, and formal integration of diverse sources of drug safety information. These advances promise to reduce delays in identifying drug-related risks, allowing earlier identification of risks as well as reassurance about the absence of specific risks.
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