Examples of 'spontaneous reporting' in a sentence
Meaning of "spontaneous reporting"
Spontaneous reporting refers to the voluntary reporting of adverse events or side effects of medications or other products by healthcare professionals or patients. It plays an essential role in pharmacovigilance, allowing the early detection and monitoring of potential safety concerns
How to use "spontaneous reporting" in a sentence
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spontaneous reporting
Spontaneous reporting systems remain the cornerstone of pharmacovigilance.
Additional adverse reactions from postmarketing spontaneous reporting.
Spontaneous reporting of remotely generated data.
Adverse reactions from spontaneous reporting.
From spontaneous reporting c.
Adverse reactions from clinical trials and spontaneous reporting.
Including spontaneous reporting data.
Side effects reports on the marketed product from spontaneous reporting.
They are based on spontaneous reporting therefore the frequencies are unknown.
Daytime sleepiness was markedly reduced as evidenced by spontaneous reporting by both patients.
This spontaneous reporting system should be particularly stringent for newly marketed medicines.
The detection of ADEs usually relies on spontaneous reporting ormedical chart reviews.
The following table presents all adverse reactions based on clinical trials and spontaneous reporting.
There are different ways of handling the spontaneous reporting of commands and events.
Spontaneous reporting from post-marketing.
See also
Serious hypersensitivity reactions have been reported from the spontaneous reporting system in the United States.
Thus, the spontaneous reporting provides minor reassurance regarding the safety of loratadine use in pregnancy.
Tabulated list of adverse reactions The reported adverse effects come from spontaneous reporting and literature.
Adverse reactions from spontaneous reporting Reporting of suspected adverse reactions.
In addition, cases of the following adverse reactions have been reported through spontaneous reporting only,.
Spontaneous reporting of suspected adverse drug reactions ( ADRs ) is a critical ongoing source of drug-safety information.
Daytime sleepiness was markedly reduced as evidenced by spontaneous reporting already after 10 days of treatment.
The following adverse reactions were reported in clinical trials and from post-marketing spontaneous reporting.
Lastly, the problem of under-reporting of ADRs in spontaneous reporting systems has been widely documented.
From spontaneous reporting ** systemic effects of inhaled corticosteroids.
Table 1 gives the adverse reactions observed from spontaneous reporting and in placebo-controlled trials.
No new or other adverse reactions have been identified from the post-marketing spontaneous reporting system.
Traceability of biologicals in spontaneous reporting systems EudraVigilance / AERS.
This result is echoed in the descriptive findings of the post-market spontaneous reporting rate data.
A major limitation of spontaneous reporting of ADR results from its being under-reported.
The other ( serious and non-serious ) adverse reactions were received by spontaneous reporting.
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Spontaneous disclosure of information on assets of illicit origin
I am not very good at spontaneous at the moment
Spontaneous really is not a thing these days
Examples of using Reporting
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Regular reporting by convention secretariats would be a requirement
Data warehouse and reporting web portal
Reporting on global observing systems for climate
