Examples of 'adverse events reported' in a sentence
Meaning of "adverse events reported"
The phrase 'adverse events reported' describes instances or incidents that are recorded or documented as negative occurrences resulting from a specific action, treatment, or intervention. These events are typically reported to capture and monitor any undesired or harmful effects, such as side effects, complications, or accidents. The reporting helps to assess the safety and risk profile of the intervention or treatment
How to use "adverse events reported" in a sentence
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adverse events reported
Serious adverse events reported in clinical trials.
There were no serious adverse events reported.
Other adverse events reported in the studies.
The following table shows the adverse events reported in the.
No serious adverse events reported were associated with sofosbuvir.
Gastrointestinal disorders were the most common adverse events reported in the studies.
There were no adverse events reported as a result of telerehabilitation interventions.
Injection site reactions represented the majority of all the adverse events reported in the trial.
There were no serious adverse events reported attnbutable to bremelanotide.
The term " n " refers to the number of adverse events reported.
There were no serious adverse events reported attributable to bremelanotide.
Further, the drug was well tolerated, with no significant drug-related adverse events reported.
Adverse events reported as serious in myelodysplastic syndromes clinical trials.
There were no serious adverse events reported in any of the groups.
Adverse events reported in adults have also been observed in adolescents.
See also
There were many other adverse events reported during the studies.
Adverse events reported during periods of placebo exposure were excluded.
This is what is leading the adverse events reported from vaccines.
Adverse events reported by treatment.
There were no drug related serious adverse events reported in any Levadex trial.
Most of the adverse events reported were described as only mild or moderate in severity.
Adverse Event Reports There were no serious adverse events reported in this trial.
There were no adverse events reported in the majority of case reports of overdose.
LFA3TIP was well tolerated with non drug-related serious adverse events reported.
The most common adverse events reported were pneumonia and pyrexia.
ACP-103 was well tolerated at both of these doses with no adverse events reported.
Adverse events reported for each of these patient populations are provided below.
CDC and FDA will continue to monitor adverse events reported after RotaTeq vaccination.
Adverse events reported in fetuses and in neonates were also summarized by treatment group.
Less common, but serious adverse events reported in the literature include.
Adverse events reported following overdosage were similar to those reported with normal vaccine administration.
Furthermore, there were no serious adverse events reported during the study or in follow-up.
The adverse events reported during this study were all of mild severity.
During the study period, the main adverse events reported generally occurred in the.
The adverse events reported are summarized irrespective of the causality assessment of the investigators.
Patient falls were the largest category of adverse events reported at Barnes - Jewish Hospital.
There were few adverse events reported across studies and those reported were relatively mild.
Under this protocol, H. pylori eradication was achieved in 39/58 patients with only mild adverse events reported.
Gastrointestinal adverse events reported were mild to moderate in severity for one subject.
All Serious treatment-emergent adverse events reported in 2 or more subjects.
Adverse events reported on Refuldan are shown in the table below.
To date, there have been no adverse events reported in Canada related to the PAP-IMI.
Adverse events reported on Refludan are shown in the table below.
Denmark reports that 24 % of the adverse events reported after HPV vaccinations were considered serious.
Adverse events reported by subject including starting point and duration ( time to resolution ).
The numbers of individual non-serious adverse events reported for each treatment are given in Table 12.
The adverse events reported were qualitatively similar to that for Ultram.
There were 84 adverse events reported.
Most adverse events reported consisted of localized reactions and non-specific symptoms.
All grade 3 or 4 treatment-emergent adverse events reported in 2 or more subjects.
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Examples of using Reported
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Riots have been reported throughout our country
Reported comments are usually taken into account
No seizures were reported for ergometrine and isosafrole
