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Table 3 Concomitant conditions

From: Safety and efficacy of favipiravir in COVID-19 patients with pneumonia. A randomized, double-blind, placebo-controlled study (FAVID)

Concomitant conditions

Favipiravir

Placebo

Total

Hypertension

N (%)

No

19 (82.61 %)

18 (85.71 %)

37 (84.09 %)

Yes

4 (17.39 %)

3 (14.29 %)

7 (15.91 %)

Total

23 (100 %)

21 (100 %)

44 (100 %)

Not available

0

0

0

Diabetes

N (%)

No

21 (91.3 %)

19 (90.48 %)

40 (90.91 %)

Yes

2 (8.7 %)

2 (9.52 %)

4 (9.09 %)

Total

23 (100 %)

21 (100 %)

44 (100 %)

Not available

0

0

0

Chronic obstructive pulmonary disease (COPD)

N (%)

No

23 (100 %)

20 (95.24 %)

43 (97.73 %)

Yes

0 (0 %)

1 (4.76 %)

1 (2.27 %)

Total

23 (100 %)

21 (100 %)

44 (100 %)

Not available

0

0

0

Cardiovascular disease

N (%)

No

23 (100 %)

20 (95.24 %)

43 (97.73 %)

Yes

0 (0 %)

1 (4.76 %)

1 (2.27 %)

Total

23 (100 %)

21 (100 %)

44 (100 %)

Not available

0

0

0

Cancer

N (%)

No

20 (86.96 %)

20 (95.24 %)

40 (90.91 %)

Yes

3 (13.04 %)

1 (4.76 %)

4 (9.09 %)

Total

23 (100 %)

21 (100 %)

44 (100 %)

Not available

0

0

0

Autoimmune disease

N (%)

No

23 (100 %)

21 (100 %)

44 (100 %)

Yes

0 (0 %)

0 (0 %)

0 (0 %)

Total

23 (100 %)

21 (100 %)

44 (100 %)

Not available

0

0

0

Neurologic disease, N (%)

No

23 (100 %)

21 (100 %)

44 (100 %)

Yes

0 (0 %)

0 (0 %)

0 (0 %)

Total

23 (100 %)

21 (100 %)

44 (100 %)

Not available

0

0

0

Other

N (%)

No

20 (86.96 %)

15 (71.43 %)

35 (79.55 %)

Yes

3 (13.04 %)

6 (28.57 %)

9 (20.45 %)

Total

23 (100 %)

21 (100 %)

44 (100 %)

Not available

0

0

0

Patients in whom concomitant conditions have affected the disease under study

N (%)

No

17 (89.47 %)

18 (94.74 %)

35 (92.11 %)

Yes

2 (10.53 %)

1 (5.26 %)

3 (7.89 %)

Total

19 (100 %)

19 (100 %)

38 (100 %)

Not available

4

2

6

  1. Table for the mITT/SAS population
  2. Percentages calculated using the total number of subjects in each treatment arm as the denominator