moderate in severity

See: mitigate
References in periodicals archive ?
All adverse events were mild to moderate in severity, with the most frequent being sedation.
Adverse events were generally mild to moderate in severity.
Most were mild or moderate in severity and only a small number of patients (less than 3%) with these side effects discontinued the study.
Adverse events were predominantly limited to the site of application (rash, pruritus, pain, and skin irritation) and were generally mild to moderate in severity.
Adverse events at least possibly related to treatment were generally mild to moderate in severity and mainly occurred at the site of application.
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