Nebenwirkungen · Trulicity
Trulicity 0.75 mg solution for injection in pre-filled pen Trulicity 1.5 mg solution for injection in pre-filled pen Trulicity 3 mg solution for injection in pre-filled pen Trulicity 4.5 mg solution for injection in pre-filled pen · Abschnitt 4.8 · PDF-Seite 10
HOS-130073 · Präparat HOS-096833
In a phase 3 study with 1.5 mg, 3 mg and 4.5 mg dulaglutide doses respectively, cumulative reporting of gastrointestinal events through to 52 weeks included nausea (14.2 %, 16.1 % and 17.3 %), diarrhoea (7.7 %, 12.0 % and 11.6 %) and vomiting (6.4 %, 9.1 % and 10.1 %). In clinical pharmacology studies conducted in patients with type 2 diabetes mellitus up to 6 weeks, the majority of gastrointestinal events were reported during the first 2-3 days after the initial dose and declined with subsequent doses.
Originalpassage; keine automatisch abgeleitete Schwere, Häufigkeit oder Kausalität. Auch verneinte Befunde und nicht untersuchte Kombinationen bleiben sichtbar.
Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2026-01-30T14:51:00Z · SHA-256 8f7c34e4753bded4db7c0494f49b503f91f5736e3b7e360143648c1ad38b32e3 · Passage 1b49dd136f1e098613c4d96cc8fa1ff4bb51e936090908ffb8fedad5f52631ca · Zeichen 6858–7366 im Abschnitt