Found 81 datasets matching "adverse events".
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Background Even though the annual incidence rate of measles has dramatically decreased in industrialised countries since the implementation of universal immunisation programmes, cases...
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Public access allowing for public search of the FDA Adverse Events Database
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A set of three proposed "hub" key events were used to link together a series of example adverse outcome pathway (AOP) descriptions that were previously not linked in an AOP network. While there...
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Background To present a protocol of a prospective, cohort study in which four groups of spinal cord injury (SCI) patients will participate. (Patients with indwelling urethral catheter;...
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(See Note below regarding 2015 data). The dataset contains hospitalization counts and rates (age 18+), statewide and by county, for 7 potentially-preventable adverse events that occur during a...
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This dataset contains the statewide composite patient safety and Adverse Events indicator (PSI) rate used to determine the “Incidence of measurable hospital-acquired conditions” rate for the Let’s...
Search relevance: 117.34 | Views last month: 0 -
This data set includes the Patient Safety and Adverse Events Composite measure (CMS Medicare PSI 90) and the individual CMS Patient Safety Indicators. CMS Medicare PSI 90 is a composite...
Search relevance: 97.87 | Views last month: 0 -
Background The "integrated safety report" of the drug registration files submitted to health authorities usually summarizes the rates of adverse events observed for a new drug, placebo...
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Background Hepatotoxicity is one of the most serious complications of highly active antiretroviral therapy (HAART). The aim of this report is to analyse an HIV infected patient on HAART...
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This blog post was posted on December 8, 2016, and was written by Susan Mayne, Ph.D., and Katherine Vierk, M.P.H..
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The Adverse Event Reporting System (AERS) is a computerized information database designed to support the FDA's post-marketing safety surveillance program for all approved drug and therapeutic...
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The Vaccine Adverse Event Reporting System (VAERS) online database on CDC WONDER provides counts and percentages of adverse event case reports after vaccination, by symptom, vaccine product,...
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The Vaccine Adverse Event Reporting System (VAERS) online database on CDC WONDER provides counts and percentages of adverse event case reports after vaccination, received since January 1990...
Search relevance: 54.71 | Views last month: 1 -
MAUDE data represents reports of adverse events involving medical devices. The data consists of all voluntary reports since June, 1993, user facility reports since 1991, distributor reports since...
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This data set provides biological information from of a captive study of transgenic mice that received either passive serum transfers from black-footed ferrets (BFFs) that were vaccinated against...
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Background Decisions on treatment are guided, not only by the potential for benefit, but also by the nature and severity of adverse drug reactions. However, some researchers have found...
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Background Rofecoxib is a cyclo-oxygenase 2 selective inhibitor. This systematic review of rofecoxib in acute pain examined studies in adults of analgesic efficacy over six hours, the...
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The dataset provides performance ratings for two outcome measures for transcatheter aortic valve replacement (TAVR) procedures: in-hospital/30-day mortality and in-hospital/30-day stroke. It...
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The Total Product Life Cycle (TPLC) database integrates premarket and postmarket data about medical devices. It includes information pulled from CDRH databases including Premarket Approvals (PMA),...
Search relevance: 50.08 | Views last month: 36