Nebenwirkungen · Docetaxel Accord
Docetaxel Accord 20 mg/1 ml concentrate for solution for infusion Docetaxel Accord 80 mg/4 ml concentrate for solution for infusion Docetaxel Accord 160 mg/8 ml concentrate for solution for infusion · Abschnitt 4.8 · PDF-Seite 13
HOS-126733 · Präparat HOS-096309
Reversible cutaneous reactions have been observed and were generally considered as mild to moderate. Reactions were characterised by a rash including localised eruptions mainly on the feet and hands (including severe hand and foot syndrome), but also on the arms, face or thorax, and frequently associated with pruritus. Eruptions generally occurred within one week after the docetaxel infusion. Less frequently, severe symptoms such as eruptions followed by desquamation which rarely lead to interruption or discontinuation of docetaxel treatment were reported (see sections 4.2 and 4.4). Severe nail disorders are characterised by hypo- or hyperpigmentation and sometimes pain and onycholysis.
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 2025-02-13T16:39:00Z · SHA-256 d97e7b4032943cf3884a7cbbb15dd1e84fa3ec25adf59d53d9e453c89968c5ae · Passage 9e3eebbce40012ff7ee736b3e5122763823f3489cfe6c62aa6853f8b973f6508 · Zeichen 4188–4883 im Abschnitt