Souvenaid vs placebo
Souvenaid showed no clear difference in any adverse events compared with placebo (moderate certainty).
- RR 0.86 [0.69, 1.07]1 study · 258 participantsModerate
Souvenaid showed no clear difference in any adverse events compared with placebo (moderate certainty).
Souvenaid showed no clear difference in any adverse events compared with placebo (moderate certainty).
Biological therapy showed no clear difference in any adverse events compared with placebo, best supportive care (BSC) or no treatment (high certainty).
Chemotherapy showed no clear difference in any adverse events compared with placebo, best supportive care (BSC) or no treatment (high certainty).
Antibiotic treatment showed no clear difference in all adverse events compared with placebo or no treatment (low certainty).
Antibiotics showed no clear difference in all adverse events compared with placebo or usual care (low certainty).
It is very uncertain whether adverse events with anti‐gram‐positive antibiotics changes any adverse events compared with placebo (very low certainty).
Thrombopoietin mimetics showed no clear difference in all adverse events compared with placebo (moderate certainty).
It is very uncertain whether azathioprine changes any adverse events compared with placebo (very low certainty).
Amitriptyline probably leads to higher overall tolerability Drop‐out due to adverse events compared with placebo (moderate certainty).
Paracetamol showed no clear difference in serious adverse events: number experiencing 24 weeks compared with placebo (moderate certainty).
Umeclidinium bromide showed no clear difference in adverse events (not including serious adverse events) compared with placebo (moderate certainty).
Mometasone/formoterol (MF/F) showed no clear difference in adverse events—serious—400/103 Duration of six months compared with placebo (low certainty).
Mometasone/formoterol (MF/F) showed no clear difference in adverse events—serious—200/103 Duration of six months compared with placebo (low certainty).
Budesonide/formoterol (BDF) showed no clear difference in adverse events—'serious'—320/94 Duration of 10 months3 compared with placebo (low certainty).
Budesonide/formoterol (BDF) showed no clear difference in adverse events—'serious'—160/94 Duration of nine months 3 compared with placebo (low certainty).
It is very uncertain whether pharmacological intervention changes adverse events (GI) compared with no intervention or placebo (very low certainty).
It is very uncertain whether benzodiazepines changes adverse events: any compared with phenobarbital (as active placebo) (very low certainty).