Maternal adverse events (6 to 8 hours) · women who have given birth vaginally, requiring analgesia for after‐birth pains.
NSAID may leads to lower maternal adverse events (6 to 8 hours) compared with opioid (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
Maternal adverse events · women who have given birth vaginally, requiring analgesia for after‐birth pains.
NSAID showed no clear difference in maternal adverse events (4 to 8 hours) compared with placebo (low certainty).
1 finding from 1 review
Unintended adverse events ‐ not reported · children aged 5 years and under
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Adverse events during treatment period · people with acute ischemic stroke
Nimodipine showed no clear difference in adverse events during treatment period compared with placebo (moderate certainty).
1 finding from 1 review
Adverse events during treatment period · people with acute ischemic stroke
Flunarizine may leads to higher adverse events during treatment period compared with placebo (low certainty).
1 finding from 1 review
Adverse events during treatment period · people with acute ischemic stroke
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Adverse events during treatment period · people with acute ischemic stroke
Other calcium antagonists showed no clear difference in adverse events during treatment period compared with placebo (low certainty).
1 finding from 1 review
Adverse events during treatment period · people with acute ischemic stroke
Calcium antagonists showed no clear difference in adverse events during treatment period compared with placebo (moderate certainty).
1 finding from 1 review
Drowsiness/somnolence (Event rate during treatment, length of treatment varied across trials) · acute mania
Lithium probably leads to lower adverse events: drowsiness/ somnolence compared with risperidone (moderate certainty).
1 finding from 1 review
Intervention not reported
Adverse events Post‐operative bleeding · participants with β‐thalassaemia
It is very uncertain whether the intervention changes adverse events Post‐operative bleeding (very low certainty).
1 finding from 1 review
Adverse events: diarrhoea and headache · people with sickle cell disease
1 finding from 1 review
Non‐serious adverse events: leukopenia · primary hepatocellular carcinoma
It is very uncertain whether TACE followed by 3‐DCRT changes non‐serious adverse events: leukopenia compared with TACE (very low certainty).
1 finding from 1 review
Serious adverse events at up to 5‐year · 9‐ to 14‐year‐old females and males
It is very uncertain whether two doses of HPV vaccine with longer interval changes serious adverse events at up to 5‐year compared with two doses of HPV vaccine with shorter interval (very low certainty).
1 finding from 1 review
Serious adverse events at up to 3‐year · 10‐ to 26‐year‐old males
It is very uncertain whether three doses HPV vaccine changes serious adverse events at up to 3‐year compared with control (very low certainty).
1 finding from 1 review
Serious adverse events at up to 5‐year · 9‐ to 15‐year‐old females
It is very uncertain whether two doses of HPV vaccine changes serious adverse events at up to 5‐year compared with three doses of HPV vaccine (very low certainty).
1 finding from 1 review
Serious adverse events: major bleeding · dialysis vascular access outcomes in AVG patients with ESKD
It is very uncertain whether omega‐3 fatty acids changes serious adverse events: major bleeding compared with placebo (very low certainty).
1 finding from 1 review
Serious adverse events: major bleeding · Dialysis vascular access outcomes in AVF patients with ESKD
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Diarrhoea · first aid in patients with acute oral poisoning (toxic berries)
Syrup of ipecac may leads to higher incidence of adverse events: diarrhoea compared with no intervention (low certainty).
1 finding from 1 review
Unintended or adverse effects · students aged 13‐19
1 finding from 1 review