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. 2022 Oct 5;9(12):ofac500. doi: 10.1093/ofid/ofac500

Table 4.

Patients With MDR TB Treated With Linezolid With ≥1 Linezolid-Related Adverse Event—California, 2009–2016

Overall (n = 69) Standard-Dose Linezolid (600 mg/d; n = 39) Low-Dose Linezolid (Intermittent Dose and 300-mg Daily Dose; n = 30) Intermittent Dose of Linezolid (n = 10) 300 mg/d of Linezolid (n = 20)
Any adverse events, No. (%) 62 (90) 33 (85) 29 (97) 10 (100) 19 (95)
Hematologic, No. (%) 49 (71) 25 (64) 24 (80) 9 (90) 15 (75)
Leukopenia, No. (%) 27 (39) 17 (25) 10 (33) 2 (20) 8 (40)
Neutropenia, No. (%) 7 (10) 4 (10) 3 (10) 1 (10) 2 (10)
Anemia, No. (%) 34 (49) 16 (44) 18 (60) 7 (70) 11 (55)
Thrombocytopenia, No. (%) 21 (30) 10 (26) 11 (37) 6 (60) 5 (25)
Neurologic, No. (%) 45 (65) 26 (67) 19 (63) 7 (70) 12 (60)
Symptoms or diagnosis of peripheral neuropathy, No. (%) 32 (46) 18 (46) 14 (47) 4 (40) 10 (50)
Optic neuropathy or visual changes, No. (%) 21 (30) 10 (26) 11 (37) 5 (50) 6 (30)
Other, No. (%) 2 (2.9) 1 (2.6) 1 (3.3) 0 (0) 1 (5)
Adverse event rate per linezolid-month on 600 mg/d 0.21 .20 0.32a 0.44 0.28
Adverse event rate per linezolid-month on low dose N/A N/A 0.10a 0.09 0.11

Abbreviation: N/A, not available; MDR TB, multidrug-resistant tuberculosis.

a

P = .03.