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. 2020 Jul 10;2020(7):CD013600. doi: 10.1002/14651858.CD013600.pub2

4. Adverse events: grade 3 or 4.

Study Number of participants Grade 3 or 4 adverse eventsa
Ahn 2020 2 0
Duan 2020b 10 (convalescent plasma group) 0
Jin 2020
   6
  0
 
 
Li 2020
  52 (convalescent plasma group)
  3 (in 2 participants)
  • 1  possible severe transfusion‐associated dyspnoea (participant had "shortness of breath, cyanosis, and severe dyspnoea within 6 hours of transfusion. The  patient was given dexamethasone, aminophylline, and other supportive care immediately and gradually improved after 2 hours").   

  • 1 non‐severe allergic transfusion reaction and 1 probable non‐severe febrile non‐haemolytic transfusion reaction (participant developed chills and rashes within 2 hours of transfusion but recovered fully after treatment with dexamethasone and promethazine).

Liu 2020
  39 (convalescent plasma group)
  0
 
Pei 2020 3 1 (anaphylactic shock)
Perotti 2020
 
  46
 
  5 (in 4 participants)
  • chills and fever during transfusion (relation likely)

  • urticaria (relation likely)

  • anaphylaxis/hypersensitivity (relation possible)

  • transfusion‐related acute lung injury (relation possible)

  • subsegmental pulmonary embolism (relation unlikely/excluded)  

Salazar 2020c
  25
  0
Tan 2020 1 1 (fever)
Ye 2020 6 0
Zeng 2020
  6 (convalescent plasma group)
  0
 
Zhang 2020ad 4 0
Zhang 2020b 1 0

aWe assume that these adverse events were grade 3 or 4, but the studies did not specify the degree of severity.
bOne participant with evanescent red face (grade unclear).
cOne participant with morbilliform rash one day post‐transfusion that lasted for several days (grade unclear).
dAssessment of adverse events only reported for one individual. Unclear information provided for the other three participants.