Nebenwirkungen · Capecitabine Accord
Capecitabine Accord 150 mg film-coated tablets Capecitabine Accord 300 mg film-coated tablets Capecitabine Accord 500 mg film-coated tablets · Abschnitt 4.8 · PDF-Seite 13
HOS-125520 · Präparat HOS-096081
ADRs considered by the investigator to be possibly, probably, or remotely related to the administration of capecitabine are listed in Table 5 for capecitabine given as monotherapy and in Table 6 for capecitabine given in combination with different chemotherapy regimens in multiple indications. The following headings are used to rank the ADRs by frequency: very common (≥ 1/10), common (≥ 1/100 to < 1/10) uncommon (≥ 1/1,000 to < 1/100), rare (≥ 1/10,000 to < 1/1,000) and very rare (< 1/10,000). Within each frequency grouping, ADRs are presented in order of decreasing seriousness.
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Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
Version 2025-05-05T15:07:00Z · SHA-256 31136a37a67bcc7d3d37a3db0a926c5402c9346bcaefe911a69ae0fa32bf9225 · Passage 2a98c615c224177110f7adc0874455e4671db9804518f8460644c58e89fcac91 · Zeichen 964–1549 im Abschnitt