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Poherdy · 4.8 · Reporting of suspected adverse reactions
Eintrag öffnenPoherdy · 4.8 · Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows con
Eintrag öffnenPoherdy · 4.8 · Summary of the safety profile
Eintrag öffnenPoherdy · 4.8 · System organ Very Common Common Uncommon Rare class Infections and Nasopharyngitis Paronychia infestations Upp
Eintrag öffnenPoherdy · 4.8 · Table 2 Summary of ADRs in patients treated with Pertuzumab in clinical trials^, and in the Post-marketing set
Eintrag öffnenPoherdy · 4.8 · Table 2 summarizes the ADRs from the pertuzumab-treated groups of the following pivotal clinical trials: • CLE
Eintrag öffnenPoherdy · 4.8 · Tabulated list of adverse reactions
Eintrag öffnenPoherdy · 4.8 · The ADRs are listed below by MedDRA system organ class (SOC) and categories of frequency: Very common (≥ 1/10)
Eintrag öffnenPoherdy · 4.8 · The incidence of the following all grade adverse events was at least 5% higher in patients ≥ 65 years of age,
Eintrag öffnenPoherdy · 4.8 · The most common ADRs (≥30%) from this pooled data were diarrhoea, alopecia, nausea, fatigue, neutropenia, and
Eintrag öffnenPoherdy · 4.8 · Within each frequency grouping and SOC, ADRs are presented in the order of decreasing seriousness.
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