Adverse effects (number of participants who had the event) · People with American cutaneous and mucocutaneous leishmaniasis
Oral miltefosine (50 mg for 28 days) probably leads to higher adverse effects (number of participants who had the event) compared with placebo (same regimen) (moderate certainty).
1 finding from 1 review
Recurrence · People with American cutaneous and mucocutaneous leishmaniasis
Oral miltefosine (50 mg for 28 days) showed no clear difference in recurrence compared with placebo (same regimen) (low certainty).
1 finding from 1 review
Blepharospasm‐specific severity ( · adults with blepharospasm
1 finding from 1 review
no estimate extracted
Studies not reported
Moderate
Adverse events (reported at any time) (2 RCT, 169 participants) · adults with blepharospasm
Botulinum toxin type A showed no clear difference in adverse events (reported at any time) (2 RCT, 169 participants) compared with placebo (low certainty).
1 finding from 1 review
RR 1.18 [0.87, 1.6]
Studies not reported
Low
Subjective evaluation of the treatments by participants · adults with blepharospasm
1 finding from 1 review
no estimate extracted
Studies not reported
High
Frequency of blepharospasm‐specific involuntary movements ( · adults with blepharospasm
1 finding from 1 review
no estimate extracted
Studies not reported
Low
Health‐related quality of life · adults with blepharospasm
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Tolerability (number of dropouts; reported at any time) (2 RCT, 169 participants) · adults with blepharospasm
Botulinum toxin type A showed no clear difference in tolerability (number of dropouts; reported at any time) (2 RCT, 169… compared with placebo (moderate certainty).
1 finding from 1 review
RR 1.44 [0.31, 6.79]
Studies not reported
Moderate
Duration of effect (when effects started to wane) · adults with blepharospasm
1 finding from 1 review
no estimate extracted
Studies not reported
Low
Relief of pain · women who have given birth vaginally, requiring analgesia for after‐birth pains.
NSAID probably leads to higher adequate pain relief as reported by the woman (5 to 8 hours) compared with placebo (moderate certainty).
1 finding from 1 review
Relief of pain · women who have given birth vaginally, requiring analgesia for after‐birth pains.
Opioid showed no clear difference in adequate pain relief as reported by the woman (5 to 8 hours) compared with placebo (low certainty).
1 finding from 1 review
Need for additional pain relief (6 to 8 hours) · women who have given birth vaginally, requiring analgesia for after‐birth pains.
Opioid may leads to lower need for additional pain relief (6 to 8 hours) compared with placebo (low certainty).
1 finding from 1 review
Maternal adverse events (6 to 8 hours) · women who have given birth vaginally, requiring analgesia for after‐birth pains.
Opioid showed no clear difference in maternal adverse events (6 to 8 hours) compared with placebo (low certainty).
1 finding from 1 review
Neonatal adverse events · women who have given birth vaginally, requiring analgesia for after‐birth pains.
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Length of hospital stay · women who have given birth vaginally, requiring analgesia for after‐birth pains.
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Additional pain relief · women who have given birth vaginally, requiring analgesia for after‐birth pains.
NSAID may leads to lower need for additional pain relief (5 to 8 hours) compared with placebo (low certainty).
1 finding from 1 review
Any breastfeeding at hospital discharge · women who have given birth vaginally, requiring analgesia for after‐birth pains.
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Any breastfeeding at 6 weeks postpartum · women who have given birth vaginally, requiring analgesia for after‐birth pains.
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Relief of pain · women who have given birth vaginally, requiring analgesia for after‐birth pains.
It is very uncertain whether paracetamol changes adequate pain relief as reported by the woman (6 hours) compared with placebo (very low certainty).
1 finding from 1 review
Need for additional pain relief (up to 4 hours) · women who have given birth vaginally, requiring analgesia for after‐birth pains.
It is very uncertain whether paracetamol changes need for additional pain relief (up to 4 hours) compared with placebo (very low certainty).
1 finding from 1 review