The phrase "adverse event case" is correct and usable in written English.
It can be used in contexts related to healthcare, clinical trials, or safety reporting, typically referring to a situation where an adverse event has been documented.
Example: "The researchers compiled an adverse event case to analyze the side effects experienced by participants during the trial."
Alternatives: "adverse incident report" or "adverse event report".
All adverse events are recorded on an adverse event case report form.
In this study, we will perform blood tests, urine analysis and adverse event case reports to confirm the safety of the proposed herbal moisturiser.
All adverse events are recorded on an adverse event case report form during study interventions and evaluated for relevance to the intervention and severity according to IRB mandated criteria by the study rheumatologist.
All adverse events, whether serious or not, were described in the source documents and Grade 2 or higher (per CTCAE 4.0) adverse events were captured on the adverse event case report forms.
Regarding research, future clinical studies should follow general recommendations for assessing and reporting harm (e.g. [ 124]) and adverse event case reports should take into account corresponding guidelines for publication (e.g. [ 125]).
All adverse events, grade II or more (according to NCI-CTCv4.0) reported spontaneously by the patient or observed by the treating physician or investigator, were recorded on an adverse event case report form.
They used the forms to follow-up the adverse event cases.
Table 2 indicates that the total adverse event cases in deanxit group were 10 and in placebo group were 11.
More than half of all adverse event cases 51-622%) are associated with surgical services [ 19, 21, 22].
A summary rate of occurrence is derived from the total of adverse event cases divided by the total of the study populations reported by our sources for each adverse effect.
In all these late-onset adverse events cases, the time between the adverse event occurrence date and that corresponding to the very high daily dose verapamil use was equal or higher than 2 years.
