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. 2016 Nov 21;60(12):7098–7104. doi: 10.1128/AAC.01044-16

TABLE 6.

Adverse events

Adverse eventa % (n)
Cirrhotic patients (n = 16) Healthy volunteers (n = 16)
Supraventricular tachycardia 6.3 (1) 0
Atrial fibrillation paroxysm 6.3 (1) 0
Premature ventricular contractions 6.3 (1) 0
Mild somnolence 6.3 (1) 0
a

These first adverse events occurred in the same patient on day 4 after a single dose of narlaprevir at 200 mg (part 1), including premature supraventricular contractions, which was considered serious and possibly related to study treatment. It developed in a 67-year-old patient with arterial hypertension and previous episodes of premature ventricular contractions in her medical history. All adverse events in this patient resolved with appropriate medical treatment.