9. Serious adverse events (SAEs).
Study | Number of participants | Serious adverse events | |
CP group | Control group | ||
Convalescent plasma versus placebo or standard care alone for individuals with moderate to severe disease | |||
Agarwal 2020 | 227 in CP group and 224 in control group |
|
NR |
AlQahtani 2020 | 20 in CP group and 20 in control group | NR | NR |
Avendano-Sola 2020 | 38 in CP group and 43 in control group |
|
|
Gharbharan 2020 | 43 in group and 43 in control group |
|
NR |
Hamdy Salman 2020 | 15 in group and 15 in control group | NR | NR |
Horby 2021 | 5795 in group and 5763 in control group |
|
NR |
Li 2020 | 52 in CP group and 51 in control group | NR |
NR |
Ray 2020 | 40 in CP group and 40 in control group | NR | NR |
Simonovich 2020 | 228 in CP group and 105 in control group |
|
|
Convalescent plasma versus standard plasma for individuals with moderate to severe disease | |||
Bajpai 2020 | 14 in CP group and 15 in control group | NR | NR |
O’Donnell 2021 | 147 in CP group an 72 in control group |
|
|
Convalescent plasma (no comparison) for individuals with moderate to severe disease | |||
Joyner 2020 | 35,322 (20,000 included in safety analysis) | Total events within 7 days after transfusion: 1282 Within 4 h after transfusion: 146 events reported
Within 7 days after transfusion: additional 1136 events reported
|
N/A (single‐arm study) |
Convalescent plasma versus placebo or standard of care alone for individuals with mild disease | |||
Libster 2020 | 80 in CP group and 80 in control group |
|
|
Abbreviations: CP: convalescent plasma; NR: not reported; TACO: transfusion‐associated circulatory overload; TRALI: transfusion‐related acute lung injury; SAEs: serious adverse events; SHOT: serious hazards of transfusion.