Приклади вживання Adverse event Англійська мовою та їх переклад на Українською
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Estimate the probability of an adverse event;
The Vaccine Adverse Event Reporting System.
Contact you for further information about the adverse event you reported;
Any adverse event affects their mood.
The FDA said it has received 194 reports of adverse event involving flavocoxid.
Adverse event has not been observed during clinical studies with Azyter.
Reported at least one adverse event(30% in the placebo group).
In the task number 27should choose the pipeline as valve associated with adverse event( wears).
A single adverse event of photophobia of 10 minutes duration was reported.
Gastrointestinal bleeding is a common adverse event seen in many patients.[6].
Based on adverse event reports of metabolic syndrome from all clinical trials with quetiapine.
For example,a pain-relief drug is tested on 1500 human subjects, and no adverse event is recorded.
(29) Based on adverse event reports of metabolic syndrome from all clinical trials with quetiapine.
In post-marketing spontaneous reporting,infections are the most common serious adverse event.
The most common adverse event that was observed in both groups, not counting the causal relationship, was infection.
The personal data that wemay collect about you when you are the subject of an adverse event report includes your:.
Hemorrhage, as an adverse event, was experienced by 15.6% of medical abortion patients compared with 2.1% for surgical patients.
However, 10% of the 29 patients in the 26-weekstudy had at least one serious adverse event, including liver toxicity.
The only consistently reported adverse event was musculoskeletal pain which is no different from the experience in the adult population.
Apart from these findings,clinical investigations in this age group do not indicate an adverse event profile different from that observed in younger patients.
The adverse event may be any unfavorable or unintended sign, abnormal laboratory finding, symptom or disease.
If you or someone in your family experience an adverse event after taking a dietary supplement, report it to the FDA.
Our legitimate business interest in managing consumer inquiries, as well as your consent for specialcategory data which may be collected in some adverse event cases.
If the person did not appreciate the likelihood of an adverse event, or he begins an affair with an extremely low chance of success, the risk is not justified.
Profession(this information may determine the questions you are asked about an adverse event, depending on your assumed level of medical knowledge).
If healthcare professionals wish to report an adverse event or product quality complaint to Ipsen Pharma, they should use the appropriate fields provided on the Website WEB.