Author and year | Significant adverse events | Severe illness symptoms | Mild illness symptoms | Sustained recovery | Patients entered ICU | Oxygen requirements |
---|---|---|---|---|---|---|
1. Benotmane et al. 2022 [38] | Â | Â | Â | Â | Only 3 of 416 patients had entered ICU | Â |
2. Kaminski et al. 2022 [45] | – | Within (333), (2) COVID-19-related hospitalization in the intensive care unit |  |  | Only 2 of 333 patients had entered the ICU in the intervention group; in the control group, six from 7 had entered the ICU |  |
3. Nguyen et al. 2022 [27] |  | – | – |  |  | 6 of 49 patients needed oxygen |
4. Lafont et al. 2022 (for prophylaxis) [28] |  | – |  |  | 1 of 15 had entered the intervention group, but two of 10 in the control group | 2 of 15 patients needed oxygen in the intervention group. However, in the control group, three out of 10 needed oxygen |
5. Lafont et al. 2022 (for treatment) [28] | Not reported | Within a total of l 42, (5) reported oxygen requirements, (12) hospitalization, (2) intensive care | Within a total of l 42, (2) reported asymptomatic, (26) fever, (28) cough, (15) dyspnea, | Â | 2 of 13 had entered the ICU in the intervention group, but two of 10 in the control group | 2 of 13 patients needed oxygen in the intervention group, but in the control group, there were three from 10 |
6. Ordaya et al., 2022 [30] | Only two individuals had severe respiratory symptoms, while other patients showed mild respiratory symptoms with no mortality | Within eight patients: (2) showed bacterial complications, and (1) needed oxygen therapy | Ranging from asymptomatic to cough, dyspnea, | Â | Â | Only one patient out of 8 needed oxygen |
7. Levin et al., 2022 (PROVENT) [11] | Total 3461 include (64) sever, (50) serious, and (93) particular interest adverse events, including (82) Injection-site reactions | – |  |  |  |  |
9. Thomas L et al.,2022 [38] ACTIV-3-(TICO) [37] | – |  |  | Of 710 patients, 17 sustained recovery in the intervention group, but 595 from 707 sustained recovery in the control |  |  |
10. Karaba et al. 2022 [46] | Through 7 days of any T+C injection, no subjects stated any adverse cardiac events, hypersensitivity reactions, or acute organ rejection (reactions that were reported were mild to moderate) | Â | Â | Â | Â | Â |
11. Jondreville et al. 2022 [41] | Only one patient of, 161 had significant adverse events | Â | Â | Â | Â | Â |
12. Calabrese et al. 2022 [37] | Only one of 412 patients had significant adverse events | Â | 11 of 412 patients had mild symptoms | Â | Â | Â |
13. Goulenok et al. 2022 [49] | Â | None from 10 patients had a severe illness in the intervention group, but in the control group, four of 7 patients had severe illness symptoms | Â | Â | Â | Â |
14. Bertrand et al. 2022 [44] | Â | Only 2 of 412 patients had severe illness symptoms in the intervention group. However, in the control group, 6 160 had severe illness symptoms | Â | Â | In the intervention group, 2 of 412 entered the ICU, but in the control group, entered the ICU | Â |