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. 2020 Feb 20;10:3116. doi: 10.1038/s41598-020-60068-5

Table 2.

Adverse events associated with NAIs in subjects from the FAERS data.

SOC terms Oseltamivir, n (%) (N = 15409) Laninamivir, n (%) (N = 84) Peramivir, n (%) (N = 345) Zanamivir, n (%) (N = 891)
Psychiatric disorders 1880 (12.20) 2 (2.38) 4 (1.16) 81 (9.09)
Gastrointestinal disorders 1786 (11.59) 18 (21.43) 22 (6.38) 56 (6.29)
General disorders and administration site conditions 1875 (12.17) 7 (8.33) 32 (9.28) 113 (12.68)
Respiratory, thoracic and mediastinal disorders 1355 (8.79) 2 (2.38) 23 (6.67) 99 (11.11)
Nervous system disorders 1169 (7.59) 6 (7.14) 25 (7.25) 99 (11.11)
Skin and subcutaneous tissue disorders 672 (4.36) 2 (2.38) 12 (3.48) 32 (3.59)
Musculoskeletal and connective tissue disorders 577 (3.74) 4 (4.76) 7 (2.03) 8 (0.90)
Cardiac disorders 609 (3.95) 0 33 (9.57) 35 (3.93)
Vascular disorders 448 (2.91) 4 (4.76) 32 (9.28) 41 (4.60)
Othersa 5038 (32.70) 39 (46.43) 155 (44.93) 327 (36.70)

FAERS, Food and Drug Administration Adverse Event Reporting System; SOC, System Organ Classes; aBlood and lymphatic system disorders, Immune system disorders, Infections and infestations, Injury, poisoning and procedural complications, Metabolism and nutrition disorders, Renal and urinary disorders, etc.