Wirkstoffe & Arzneimittelsicherheit

Nebenwirkungen · Remsima

Remsima 100 mg powder for concentrate for solution for infusion · Abschnitt 4.8 · PDF-Seite 15

HOS-127142 · Präparat HOS-096377

Table 1 lists ADRs based on experience from clinical studies as well as adverse reactions, some with fatal outcome, reported from post-marketing experience. Within the organ system classes, adverse reactions are listed under headings of frequency using the following categories: 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); very rare (< 1/10,000), not known (cannot be estimated from the available data). Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness.

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