TABLE 2.

Adverse events during the 12-week study

AEa	Result for enrolled UC patients (n = 22)b
Total AEs, n	6
Total SAEs, n (%)	0 (0)
Withdrawal due to FMT-related AE, n (%)	1 (4.5)
Abdominal pain, n (%)	2 (9.1)
Loose stools, n (%)	2 (9.1)
Vomiting, n (%)	0 (0)
Fecal with capsules, n (%)	1 (4.5)

^aAE, adverse event; SAEs, serious adverse events.

^bData are number of events or number of patients with percentage shown in parentheses.