Adverse events · women with primary dysmenorrhoea
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Requirement for additional medication · women with primary dysmenorrhoea
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Time off school or work · women with primary dysmenorrhoea
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Pain improvement (assessed as improvement from 1 major category to next) · women with primary dysmenorrhoea
Combined OCP may leads to higher pain improvement (assessed as improvement from 1 major category to… compared with placebo or no treatment (low certainty).
1 finding from 1 review
Adverse events · women with primary dysmenorrhoea
Combined OCP probably leads to higher adverse events compared with placebo or no treatment (moderate certainty).
1 finding from 1 review
Requirement for additional medication · women with primary dysmenorrhoea
Combined OCP may leads to lower requirement for additional medication compared with placebo or no treatment (low certainty).
1 finding from 1 review
Time off school or work · women with primary dysmenorrhoea
Combined OCP may leads to lower absence from work or school compared with placebo or no treatment (low certainty).
1 finding from 1 review
Pain score ( · women with primary dysmenorrhoea
1 finding from 1 review
Pain improvement · women with primary dysmenorrhoea
Combined low‐dose OCP showed no clear difference in pain improvement compared with another combined low‐dose OCP (moderate certainty).
1 finding from 1 review
Adverse events for continuous vs standard regimen OCP · women with primary dysmenorrhoea
Combined low‐dose OCP may leads to higher adverse events for continuous vs standard regimen OCP compared with another combined low‐dose OCP (low certainty).
1 finding from 1 review
Requirement for additional medication · women with primary dysmenorrhoea
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Disease‐specific quality of life · Adults with overactive bladder (OAB)
Anticholinergics showed no clear difference in mean change from baseline in condition‐specific quality of lifeScale… compared with placebo (low certainty).
1 finding from 1 review
Perception of improvement or cure · Adults with overactive bladder (OAB)
Anticholinergics probably leads to higher patient perception of cure or improvement compared with placebo (moderate certainty).
1 finding from 1 review
Number of urgency episodes per 24 hours: immediately after treatment · Adults with overactive bladder (OAB)
Anticholinergics showed no clear difference in mean number of urgency episodes per 24 hours compared with placebo (moderate certainty).
1 finding from 1 review
Adverse effects: dry mouth · Adults with overactive bladder (OAB)
Anticholinergics may leads to higher adverse events: dry mouth compared with placebo (low certainty).
1 finding from 1 review
Adverse events:urinary retention · Adults with overactive bladder (OAB)
Anticholinergics may leads to higher adverse events:urinary retention compared with placebo (low certainty).
1 finding from 1 review
Withdrawals due to adverse events · Adults with overactive bladder (OAB)
Anticholinergics may leads to higher withdrawal due to adverse events compared with placebo (low certainty).
1 finding from 1 review
Number of micturition episodes per 24 hours: immediately after treatment · Adults with overactive bladder (OAB)
Anticholinergics showed no clear difference in mean number of micturitions per 24 hours compared with placebo (moderate certainty).
1 finding from 1 review
Mean daily rating of problem severity (lower score is better) · women with premenstrual syndrome (most met DSM‐V criteria for premenstrual dysphoric disorder (PMDD))
1 finding from 1 review
Mean change in daily rating of functional impairment: reduction of productivity (lower score is better) · women with premenstrual syndrome (most met DSM‐V criteria for premenstrual dysphoric disorder (PMDD))
1 finding from 1 review