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The phrase "adverse event of a" is correct and usable in written English.
It can be used in contexts related to healthcare, research, or risk management when discussing negative occurrences or incidents.
Example: "The study aimed to identify the adverse event of a new medication on patients' health."
Alternatives: "negative occurrence of a" or "unfavorable incident of a".
Exact(4)
Seven treated eyes and 14 observed eyes had an adverse event of a > or =6-line loss in VA in the absence of late age-related macular degeneration or cataract.
Three rules were describing an adverse event of a medication (For example: Bisoprolol → nausea and vomiting).
The implication of not allowing for prescribing trends would likely be an underestimate of a potential adverse event of a medicine.
Four studies reported that there were no adverse events and one study [ 58] reported one adverse event of a participant with a history of back problems, who experienced a back spasm in yoga class.
Similar(56)
Bradycardia is an expected adverse event of any heart rate-reducing treatment.
The objective of the study was to evaluate the contraceptive performance, acceptability, side effects, and adverse events of a novel "frameless" intrauterine drug delivery system (IUS), FibroPlant-levonorgestrel (LNG) releasing 14 μg of LNG/day, in perimenopausal women.
In targeted radiotherapy, patient-specific dosimetry is essential for both the prediction of the adverse events of a treatment and of the tumour response (24).
Adverse events of a mainly respiratory nature were associated with the falls in FEV1, primarily in the COPD cohort.
The adverse event rates observed in the randomised controlled trials were adjusted by assuming that halving the dose results in a reduction in adverse events of a quarter.
UB=upper boundary (80% and 99% upper boundaries of the predicted number of coincident adverse events can assess the likelihood that adverse events of a given type are not only temporally, but also causally associated with a vaccine dose).
In the varenicline group, one participant experienced moderate postoperative haemorrhage considered unrelated to the study drug and one experienced two serious adverse events of a loss of consciousness and a resultant traffic incident.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com