Reslizumab intravenous (IV) vs placebo
Reslizumab intravenous (IV) showed no clear difference in serious adverse events compared with placebo (high certainty).
- Risk ratio 0.79 [0.56, 1.12]4 studies · 1656 participantsHigh
Reslizumab intravenous (IV) showed no clear difference in serious adverse events compared with placebo (high certainty).
Reslizumab subcutaneous (SC) showed no clear difference in serious adverse events compared with placebo (high certainty).
Benralizumab subcutaneous (SC) leads to lower serious adverse events compared with placebo (high certainty).
Mepolizumab subcutaneous (SC) showed no clear difference in serious adverse events compared with placebo (high certainty).
Autologous myeloablative selective HSCT showed no clear difference in serious adverse events compared with cyclophosphamide (moderate certainty).
Autologous non‐myeloablative selective HSCT probably leads to higher serious adverse events compared with cyclophosphamide (moderate certainty).
The review found no eligible studies for this question.
The review found no eligible studies for this question.
The review found no eligible studies for this question.
The review found no eligible studies for this question.
The review found no eligible studies for this question.
The review found no eligible studies for this question.
Summary of findings table ‐ Stem Cell showed no clear difference in serious Adverse Events compared with placebo or Control (low certainty).
28 days on/off antibiotic regimen showed no clear difference in serious adverse events compared with 28 days on/off placebo regimen (low certainty).
14 days on/off antibiotic regimen showed no clear difference in serious adverse events compared with 28 days on/off antibiotic regimen (moderate certainty).
14 days on/off antibiotic regimen showed no clear difference in serious adverse events compared with 14 days on/off placebo regimen (high certainty).