Nebenwirkungen · Spedra
Spedra 200 mg tablets · Abschnitt 4.8 · PDF-Seite 34
HOS-127526 · Präparat HOS-096405
Summary of the safety profile The safety profile of Spedra is based on 2,566 subjects exposed to avanafil during the clinical development program. The most common adverse reactions reported in clinical studies were headache, flushing, nasal and sinus congestion and back pain. Overall adverse events and adverse reactions for avanafil-treated subjects were more frequent in subjects with a Body Mass Index (BMI) <25 (normal BMI subjects).
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 2026-08-07T15:55:00Z · SHA-256 9f3a1264ef001d577393feb260b99952ed079148f452f8976f0be132f469d380 · Passage 221d53a313d982dc4fe1da501fc489a3823f4ab3211c27eb90a9a4303d7a5fcc · Zeichen 0–438 im Abschnitt