In LixiLan-O patients with type 2 diabetes, 27.5% of lixisenatide-alone recipients experienced gastrointestinal adverse events during the initial treatment weeks.
In plain wordsDuring the initial treatment weeks, 27.5% of patients receiving lixisenatide alone reported stomach or bowel side effects.
- Peptide
- Lixisenatide
- Outcome
- Not applicableInitial gastrointestinal adverse-event incidence
- Study
n: not reported in source
- Outcome group
- Gastrointestinal adverse events · Gastrointestinal
- Studied dose
- Dose not stated
Measurements
- GI adverse-event incidence
- 27.5%
- lixisenatide alone, LixiLan-O
Source sentences
In iGlarLixi-treated patients, the rate of GI AEs during the initial weeks of treatment was lower versus patients treated with lixisenatide alone (9.6% and 11.7% of iGlarLixi-treated patients in LixiLan-L and LixiLan-O, respectively, vs. 27.5% of lixisenatide-treated patients in LixiLan-O).