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The phrase "adverse event reporting" is correct and usable in written English.
It can be used in contexts related to healthcare, clinical trials, or safety monitoring to refer to the process of documenting and analyzing negative occurrences or side effects associated with a treatment or intervention.
Example: "The pharmaceutical company is committed to thorough adverse event reporting to ensure patient safety and regulatory compliance."
Alternatives: "incident reporting" or "safety event documentation".
Exact(60)
The system also streamlines adverse event reporting.
This article summarizes the issue of adverse event reporting in HSCT.
Adverse event reporting systems allow healthcare institutions to detect and prevent recurrence of avoidable patient harm.
Context: The vaccine adverse event reporting system (VAERS) monitors vaccine safety post-licensure.
Errors, limitations and improvement opportunities observed when contracts are linked to indicators, information and adverse event reporting systems are analysed.
Adverse event reporting is highly variable and nonstandardized in urologic literature, especially for robot-assisted radical cystectomy (RARC).
The kit comes with consent forms, adverse event reporting guidelines, and a list of outcome variables.
Pfizer's response to the report said: "It is important to understand the limitations of spontaneous adverse event reporting.
Moreover, policy and completeness of adverse event reporting changed during the last 20 years and differ between the trials.
Tolerability was evaluated by adverse event reporting.
Safety endpoints include adverse event reporting.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com