adverse


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Related to adverse: averse, Adverse Action

adverse

opposing the interests of the patient.

adverse drug reaction (ADR)
an undesirable and unintentional effect caused by a drug administered at the normal therapeutic dose.
adverse food reaction
an abnormal response to ingested food components. It may be immunologic or non-immunologic. See also food.
adverse syndrome
lesions of the rostral thalamus causing head turning, circling or deviation of the eyes toward the side of the lesion.
References in periodicals archive ?
President Clinton has asked government funded health plans and facilities to adopt procedures to report and address adverse events.
AppOne's new feature consists of an automated module that prompts dealers to construct and print the fully compliant adverse action notice based on loan application information previously submitted.
tobacco smoke, pathogens, paint fumes, other air pollutants) could cumulatively induce adverse health effects.
There were no significant differences in the frequencies of stillbirth or other adverse pregnancy outcomes between women who had received monotherapy and those who had received multiple drug treatment.
MEDWatch is not just a new FDA system; it is a way of making reporting of adverse events and product problems a part of the culture of health care providers," said FDA Commissioner David A.
Professional societies must report adverse actions regarding members.
adverse trends in claim severity or frequency and the uncertainties in estimating property and casualty losses;
We believe the data will be viewed by clinicians as clinically important in improving patient outcomes by reducing the overall incidence of adverse cardiovascular outcomes associated with bypass surgery, and this data formed the basis for our regulatory submissions to the authorities in the U.
Renal adverse events were uncommon at 96 weeks, which is consistent with study data at 48 weeks and results from other randomized clinical trials involving Viread in treatment-naove and treatment-experienced patients.
Serious adverse events that occurred in CD patients receiving TYSABRI included intestinal obstruction, hypersensitivity reactions, abscesses, gastroenteritis, intestinal adhesions and gallstones.
Secondary endpoints included incidence of transfusions, changes in patient-reported outcomes, and incidence of adverse events and serious adverse events.