Examples of 'reported adverse events' in a sentence
Meaning of "reported adverse events"
Reported adverse events: Instances of negative or undesirable occurrences that have been officially documented, recorded, or reported
How to use "reported adverse events" in a sentence
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reported adverse events
The rate of reported adverse events was low.
Medication errors account for a significant proportion of reported adverse events.
All reported adverse events were mild or moderate in nature.
In adults there was no increased risk of reported adverse events in trials.
The only reported adverse events were generally mild in severity.
Nasopharyngitis and headache were the two most frequently reported adverse events.
The most frequently reported adverse events were of gastrointestinal origin.
The major reasons for trial discontinuation were withdrawal of consent and reported adverse events.
Reported adverse events include both local and systemic reactions.
Infections were the most commonly reported adverse events in patients with pJIA.
The reported adverse events will be coded according to MedDRA terminology.
This federal office is responsible for maintaining a national database of all reported adverse events.
Officially reported adverse events represent only a small fraction of actual events.
MedDRA terminology has been used to classify reported adverse events for bipolar depression.
All studies reported adverse events for the oestrogen treatment groups.
See also
Represents the incidence of laboratory findings, not of reported adverse events.
There were no reported adverse events or safety concerns in the course of the study.
However, only three of the five included studies reported adverse events.
The most frequently reported adverse events were associated with the injection procedure.
Also, none of the spouses involved in the studies reported adverse events.
We reported adverse events in a narrative way and included skin irritation or contact allergy.
In the following section, the frequencies of less commonly reported adverse events are presented.
The reported adverse events were consistent with the established safety profile in older children.
Safety was assessed from vital signs, clinical laboratory assessments, and reported adverse events.
More subjects reported adverse events after administration in the fasted than in the fed state.
The majority of trials that involved antidepressant medication reported adverse events including suicide-related behaviours.
Reported adverse events are listed below, by system organ class and by frequency.
Aganirsen 's safety was excellent, without any reported adverse events.
Others have been reported adverse events during the use of Minesse.
Reported adverse events were classified using standard WHO-based dictionary terminology.
Only 20 studies reported adverse events.
Most reported adverse events were not unexpected, mainly gastro-intestinal disorders or cutaneous disorders.
The most frequently reported adverse events were nausea, diarrhoea and headache.
The most commonly reported adverse events are dizziness, sensory disturbances, sleep disturbances, anxiety and headache.
Out of these, 21 reported adverse events following immunisation.
These reported adverse events occurred at an incidence of 2 % or less.
The most commonly reported adverse events were nausea, vomiting, headache and pruritus.
The majority of the reported adverse events were relatively minor, and the incidences were low.
The most frequently reported adverse events were rashes, possible vaccine failures, and injection site reactions.
Finally, three studies reported adverse events including diarrhoea, wheezing shortly after administration and rash.
The most frequently reported adverse events included headache, loose stool, lightheadedness, dizziness, and nausea.
Spontaneously reported adverse events summarized in 5 Periodic Safety Update Reports (PSURs).
The most frequently reported adverse events are headache and dyspepsia ( 11 and 7 % of cases, respectively ).
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No seizures were reported for ergometrine and isosafrole
