Skip to main content

Table 5 Treatment-Emergent Adverse Events reported by Two or More Subjects

From: Pharmacokinetics and pharmacodynamics of HTD1801 (berberine ursodeoxycholate, BUDCA) in patients with hyperlipidemia

Adverse Event

Placebo

BUDCA Dose

500 mg/day

1000 mg/day

2000 mg/day

Number of Subjects

12

12

12

14

Headache

5

5

4

3

Dizziness

0

2

0

0

Nausea

1

3

1

0

Flatulence

2

0

0

0

Anorexia

0

0

3

1