Nebenwirkungen · Revlimid
Revlimid 2.5 mg hard capsules Revlimid 5 mg hard capsules Revlimid 7.5 mg hard capsules Revlimid 10 mg hard capsules Revlimid 15 mg hard capsules Revlimid 20 mg hard capsules Revlimid 25 mg hard capsules · Abschnitt 4.8 · PDF-Seite 41–42
HOS-117202 · Präparat HOS-094537
41 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.
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Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-09-09T12:08:00Z · SHA-256 0f6cca94a1a136a03ce79918070d9d16a6919ff303eae396136f3a6bdce58c5c · Passage a23f17e6b1348c3275e247f11b749e5b9dc72b8ec8ad8639e9e97d6c9e31964f · Zeichen 67374–67733 im Abschnitt