Nausea · women with perineal pain following childbirth
Paracetamol (single administration, any dose) showed no clear difference in maternal drug adverse effects (nausea) compared with placebo (low certainty).
1 finding from 1 review
Maternal drug adverse effects (sleepiness) · women with perineal pain following childbirth
Paracetamol (single administration, any dose) showed no clear difference in maternal drug adverse effects (sleepiness) compared with placebo (low certainty).
1 finding from 1 review
Neonatal drug adverse effects · women with perineal pain following childbirth
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Change in cramp severity (0 to 10 VAS; higher = worse pain) (after 6 weeks) · older adults with lower limb muscle cramps
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Proportion of participants experiencing cramps · older adults with lower limb muscle cramps
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Health‐related quality of life · older adults with lower limb muscle cramps
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Quality of sleep · older adults with lower limb muscle cramps
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Activities of daily living · older adults with lower limb muscle cramps
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Cramp frequency (number of cramps in preceding week) (after 6 weeks) · older adults with lower limb muscle cramps
1 finding from 1 review
Adverse events · older adults with lower limb muscle cramps
1 finding from 1 review
Severe cases of rotavirus diarrhoea · children
Rotarix leads to lower severe cases of rotavirus diarrhoea compared with placebo (high certainty).
6 findings from 1 review
RR 0.07 [0.03, 0.18]
4 studies · 14976 participants
High
RR 0.42 [0.28, 0.61]
4 studies · 15822 participants
High
RR 0.65 [0.51, 0.83]
2 studies · 13768 participants
Moderate
Show 3 more findings
RR 0.1 [0.07, 0.14]
6 studies · 18145 participants
High
RR 0.21 [0.16, 0.29]
4 studies · 31671 participants
High
RR 0.23 [0.17, 0.29]
3 studies · 23834 participants
High
Severe cases of all‐cause diarrhoea · children
Rotarix leads to lower severe cases of all‐cause diarrhoea compared with placebo (high certainty).
6 findings from 1 review
RR 0.64 [0.52, 0.79]
2 studies · 26479 participants
High
RR 0.74 [0.5, 1.09]
2 studies · 23317 participants
Low
RR 0.73 [0.56, 0.95]
2 studies · 5639 participants
High
Show 3 more findings
RR 0.83 [0.72, 0.96]
1 study · 2764 participants
High
RR 0.48 [0.37, 0.61]
1 study · 3874 participants
Moderate
RR 0.49 [0.4, 0.6]
2 studies · 6269 participants
Moderate
All‐cause death · children
Rotarix showed no clear difference in all‐cause death compared with placebo (moderate certainty).
3 findings from 1 review
RR 1.27 [0.89, 1.81]
9 studies · 77043 participants
Moderate
RR 0.88 [0.63, 1.21]
11 studies · 8374 participants
Moderate
RR 0.71 [0.17, 2.88]
10 studies · 20361 participants
Low
All serious adverse events · children
Rotarix leads to lower all serious adverse events compared with placebo (high certainty).
3 findings from 1 review
RR 0.85 [0.76, 0.95]
9 studies · 77069 participants
High
RR 0.9 [0.77, 1.05]
10 studies · 7674 participants
High
RR 0.89 [0.72, 1.1]
12 studies · 18971 participants
High
Serious adverse events: intussusception · children
Rotarix showed no clear difference in serious adverse events: intussusception compared with placebo (low certainty).
3 findings from 1 review
RR 0.72 [0.39, 1.32]
6 studies · 75540 participants
Low
RR 1.49 [0.06, 36.63]
5 studies · 17068 participants
Low
RR 1.42 [0.52, 3.87]
10 studies · 20773 participants
Low
Severe cases of rotavirus diarrhoea · children
RotaTeq leads to lower severe cases of rotavirus diarrhoea compared with placebo (high certainty).
6 findings from 1 review
Show 3 more findings
RR 0.21 [0.11, 0.41]
1 study · 3863 participants
Low
RR 0.43 [0.29, 0.64]
2 studies · 6775 participants
High
RR 0.56 [0.41, 0.77]
2 studies · 6744 participants
High
Severe cases of all‐cause diarrhoea · children
The review found no eligible studies for this question.
6 findings from 1 review
no estimate extracted
Studies not reported
No studies found
no estimate extracted
Studies not reported
No studies found
no estimate extracted
Studies not reported
No studies found
Show 3 more findings
All‐cause death · children
RotaTeq showed no clear difference in all‐cause death compared with placebo (low certainty).
3 findings from 1 review
RR 1.24 [0.69, 2.22]
6 studies · 72654 participants
Low
RR 0.33 [0.01, 8.18]
2 studies · 4088 participants
Very low
RR 0.91 [0.68, 1.23]
3 studies · 7706 participants
Moderate
All serious adverse events · children
RotaTeq showed no clear difference in all serious adverse events compared with placebo (high certainty).
3 findings from 1 review
RR 0.92 [0.84, 1.01]
5 studies · 70690 participants
High
RR 0.66 [0.14, 3.17]
2 studies · 4082 participants
Very low
RR 0.99 [0.72, 1.36]
4 studies · 7730 participants
Moderate
Serious adverse events: intussusception · children
RotaTeq showed no clear difference in serious adverse events: intussusception compared with placebo (low certainty).
3 findings from 1 review
RR 0.69 [0.35, 1.38]
9 studies · 73925 participants
Low
RR 5.01 [0.24, 104.29]
2 studies · 4082 participants
Very low
RR 0.33 [0.01, 8.16]
2 studies · 7488 participants
Low