Examples of 'serious adverse event' in a sentence
Meaning of "serious adverse event"
describes a significant negative occurrence or incident that can have severe consequences or implications. It is often used in medical or clinical contexts to refer to unexpected or harmful side effects of a treatment or medication
How to use "serious adverse event" in a sentence
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serious adverse event
Serious adverse event in the placebo arm.
Three patients experienced a serious adverse event.
This serious adverse event led to prolonged hospitalization.
Three subjects reported a serious adverse event.
No serious adverse event or death occurred during the study.
Hepatotoxicity is a common and potentially serious adverse event.
Description of serious adverse event or reaction.
Simeprevir may have beneficial effects on risk of serious adverse event.
One rare potentially serious adverse event is a serotonin syndrome.
All were mild or moderate in severity and none were reported as a serious adverse event.
The most frequent serious adverse event was worsening of asthma.
There was no difference in the proportion of participants who had a serious adverse event.
No injection site reaction was reported as a serious adverse event or required treatment discontinuation.
The most serious adverse event associated with its use is hyperlipidemia.
Ystems of traceability and reporting of serious adverse event and reactions.
See also
This serious adverse event was considered unlikely to be related to the study drug.
The perspective of patients and relatives when a serious adverse event has occurred.
Frequency of a clinically serious adverse event by time of occurrence for all subjects studied.
Also, none of the trial participants reported a serious adverse event.
No vaccine relate serious adverse event was reported during the entire study period.
Participating treating physicians will have to be trained on serious adverse event detection and reporting.
A rare serious adverse event resulting from improper vaccine preparation and injection practices.
No RCT reported any serious adverse event.
The risk of a serious adverse event can increase with the duration of treatment with naproxen.
In postmarketing spontaneous reporting, infections are the most common serious adverse event.
Promptly report serious adverse event to Manufacturer.
In clinical trials, a distinction is made between an adverse event and a serious adverse event.
The only other serious adverse event was experienced by a subject in the Q group.
One patient was withdrawn due to a disease-related serious adverse event prior to the restaging scan.
What serious adverse event did the patient experience?
Favorable safety profile with no drug-related serious adverse event and no dose-limiting toxicity.
No serious adverse event attributed to TroVax ® by investigators or the sponsor has been reported.
The proportion of individuals experiencing a serious adverse event with the implanted sensor was less than 1 %.
Serious adverse event Any adverse event that,.
Safety and tolerability, There was no serious adverse event during the study.
There was one serious adverse event ( a mild infusion reaction ) probably related to the trial medication.
Grade III-IV GVHD will be reported as a serious adverse event.
Patients with > 1 serious adverse event possibly related to study drug.
One person out of 100 people taking methotrexate had a serious adverse event.
No Promptly report serious adverse event to CBS / HQ.
A serious adverse event ( experience ) or reaction is any untoward medical occurrence that at any dose,.
A healthcare professional / hospital will report a serious adverse event to Canadian Blood Services or Héma-Québec.
Patient 165 experienced intractable vomiting and was hospitalized due to this serious adverse event.
Only one single serious adverse event was available for evaluation of safety ( very low-quality evidence ).
Whether it constitutes a serious adverse event ( SAE ).
The most serious adverse event was meningococcal septicaemia in two vaccinated PNH patients see section 4.4.
One patient was not evaluable due to a serious adverse event ( SAE ) on study day 2.
Date of serious adverse event year/month/day.
Onset date and time of serious adverse event or reaction yyyy / mm / dd / hh / mm.
A serious adverse event ( SAE ) is an adverse event that,.
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