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Adverse outcomes in mothers, such as high rates of cesarean section, puerperal infections, and complication during childbirth, have been identified; and adverse outcomes also in the fetus, such as premature birth, low birth weight and small size for gestational age have been identified also.
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Depending on the hazard, overexposure can be difficult to identify and adverse health effects may not be detected for many years.
Potentially confounding determinants, such as age, sex, comorbidity, life-expectance and quality of the patient record, were identified and differences in adverse event rates between groups were adjusted for potentially confounding determinants using multilevel multivariate analysis.
This involves identifying and managing adverse effects that manifest both mentally and physically.
Based on EPA's Biomonitoring Framework for human health research, such observations are intended to link environmental exposures to a cascade of biomarker chemicals to help identify and clarify adverse outcome pathways within the context of systems biology.
The Patient Safety Learning System is an electronic system designed to help identify and manage adverse events.
The system automatically identifies and minimizes adverse drug effects due to antibiotics [ 18, 19] and has reduced inadequate administration compared with physician prescribing patterns [ 20].
For example, Weingart et al. elicited incident reports from hospital inpatients in order to identify and characterize adverse events and near misses [ 6].
The public interest for patient safety has led to a number of potentially valuable initiatives to identify and prevent adverse events.
There is also considerable interest in using claims to identify adverse events related to treatment [ 14- 17], and this interest may well strengthen with the availability of Medicare Part D oral drug data, and as the United States Food and Drug Administration explores new data structures and methodologies for identifying and analyzing adverse drug events [ 25].
The doctor has an ethical duty to inform the patient of each unwanted event and its causes, and to identify and report adverse events, near misses and procedural and diagnostic errors [ 26].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com