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

Table 5.

Characteristics of Adverse Events Among Patients With MDR TB Treated With Linezolid—California, 2009–2016

Adverse Event Severity, No. (%) Attributed to Linezolid, No. (%) Days Before Occurrence, Median (Range) Linezolid Held Due to AE, No. (%) Linezolid Discontinued Due to AE, No. (%) Linezolid Dose Reduced Due to AE, No. (%) Medical Management, No. (%) Documented Resolution, No. (%)
Hematologic (n = 89) N/A 30 (34) 46 (9–755) 31 (35) 9 (10) 16 (18) 10 (11) 62 (70)
Anemia (n = 34) Mild: 18 (53); Moderate: 10 (29); Severe: 6 (18) 17 (50) 37.5 (9–755) 12 (35) 6 (18) 8 (24) 8 (24) 15 (44)
Leukopenia (n = 37) N/A 1 (3.7) 62 (13–366) 8 (30) 1 (3.7) 2 (7.4) 1 (3.7) 23 (85)
Thrombocytopenia (n = 21) Mild: 16 (76); Moderate: 3 (14); Severe: 2 (9.5) 10 (48) 30 (13–30) 8 (38) 2 (9.5) 6 (29) 0 (0) 18 (86)
Neutropenia (n = 7) Mild: 5 (71); Moderate: 2 (29); Severe: 0 (0) 2 (29) 94 (25–379) 3 (43) 0 (0) 0 (0) 1 (14) 6 (86)
Neurologic (n = 61) N/A 27 (44) 119.5 (0–820) 24 (39) 23 (38) 12 (20) 25 (41) 22 (36)
Symptoms or diagnosis of peripheral neuropathy (n = 34) N/A 20 (59) 119.5 (24–820) 12 (35) 15 (44) 7 (21) 19 (56) 8 (24)
Vision changes or optic neuropathy (n = 25) N/A 6 (24) 163 (0–668) 11 (44) 8 (32) 5 (20) 5 (20) 12 (48)
Other (n = 2) N/A 1 (50) 24 (10–38) 1 (50) 0 (0) 0 (0) 1 (50) 2 (100)

Abbreviations: AE, adverse event; N/A, not available; MDR TB, multidrug-resistant tuberculosis.