Safety

Vistogard® (uridine triacetate)—a documented safety profile1

Adverse reactions occurring in >2% of patients (N=135)1
Adverse reaction Number of patients Percent of patients
Vomiting 13 10%
Nausea 7 5%
Diarrhea 4 3%
  • No contraindications, warnings, precautions, or cytochrome P450 drug–drug interactions1
  • May be taken without regard to meals1
  • Pharmacokinetics were not significantly affected by gender or age (in patients aged 20 to 83 years)1
  • Geriatric patients: Of the 135 patients in clinical studies with VISTOGARD, 30% were ≥65, including 11% ≥751
  • One patient receiving VISTOGARD experienced grade 3 nausea and vomiting1
  • VISTOGARD was discontinued for adverse reactions in 2 patients (1.4%)1

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