Nebenwirkungen · Twinrix Adult
Twinrix Adult, suspension for injection in pre-filled syringe Hepatitis A (inactivated) and hepatitis B (rDNA) (HAB) vaccine (adsorbed). · Abschnitt 4.8 · PDF-Seite 5
HOS-085930 · Präparat HOS-083226
The safety profile presented below is based on a pooled analysis of events per dose from more than 6,000 subjects who received either the standard 0, 1, 6 month schedule (n=5,683) or the accelerated 0, 7, 21 days schedule (n=320). The most commonly reported adverse reactions following Twinrix Adult administration with the standard 0, 1, 6 month schedule are pain and redness occurring in a per dose frequency of 37.6% and 17.0% respectively.
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 2026-08-04T10:50:00Z · SHA-256 a6c42f246f9166fd7e859c1877e94342dffe4df1f7128d39d09ec7fe44fefefe · Passage 85ab6eeab2728e1f169d7630f7b13b651b8b38ca6f804541fa10ab658f226d4c · Zeichen 31–474 im Abschnitt