Outcomes | Anticipated absolute effects* (95% CI) | Relative effect (95% CI) |
№ of participants (studies) |
Certainty of the evidence (GRADE) |
|
---|---|---|---|---|---|
Risk with placebo | Risk with Monoclonal antibodies | ||||
Symptomatic COVID-19 assessed with: positive PCR test plus COVID-19 symptoms follow-up: median 28 days |
7 per 100 | 5 per 100 (2 to 10) |
RR 0.75 (0.36 to 1.54) |
2471 (2 RCTs) |
⨁◯◯◯ Very lowa,b,c |
Symptomatic and asymptomatic COVID-19 assessed with: Positive PCR test with or without COVID-19 symptoms follow-up: median 28 days |
18 per 100 | 9 per 100 (4 to 21) |
RR 0.52 (0.23 to 1.17) |
2471 (2 RCTs) |
⨁◯◯◯ Very lowa,d,e |
All-cause mortality follow-up: median 28 days |
1 per 100 | 1 per 100 (0 to 3) |
RR 0.83 (0.25 to 2.70) |
966 (1 RCT) |
⨁⨁◯◯ Lowf |
COVID-19 related death follow-up: median 28 days |
1 per 100 | 0 per 100 (0 to 2) |
RR 0.11 (0.01 to 2.05) |
966 (1 RCT) |
⨁⨁◯◯ Lowg |
Viral load reduction from baseline assessed with: log10 follow-up: median 28 days |
The mean viral load reduction from baseline was -0.39 log10 | MD 0.8 log10 lower (1.21 lower to 0.39 lower) |
- | 132 (1 RCT) |
⨁⨁⨁◯ Moderateh |
Any adverse events follow-up: median 28 days |
26 per 100 | 22 per 100 (14 to 33) |
RR 0.85 (0.56 to 1.28) |
3792 (2 RCTs) |
⨁◯◯◯ Very lowa,i |
Serious adverse events follow-up: median 28 days |
2 per 100 | 2 per 100 (1 to 3) |
RR 0.93 (0.55 to 1.58) |
3792 (2 RCTs) |
⨁⨁⨁◯ Moderatea |
Bacteremia follow-up: median 28 days |
2 per 100 | 1 per 100 (1 to 2) |
RR 0.70 (0.37 to 1.33) |
2680 (2 RCTs) |
⨁⨁⨁◯ Moderatea |