Nebenwirkungen · Puregon
Puregon 300 IU/0.36 mL solution for injection Puregon 600 IU/0.72 mL solution for injection Puregon 900 IU/1.08 mL solution for injection · Abschnitt 4.8 · PDF-Seite 8–9
HOS-085468 · Präparat HOS-083121
8 Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the national reporting system listed in Appendix V.
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 2025-12-18T17:19:00Z · SHA-256 3fdd9364877a2ca4d9363213024887fcf6c4c693365f766eb9532291d20f6770 · Passage e1f152f06dd88ccce836ffcfc5dc411f53b5b502d53560e686a46b26c0215219 · Zeichen 4861–5219 im Abschnitt