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Mysildecard · 4.8 · In the two placebo-controlled studies adverse events were generally mild to moderate in severity. The most com
Eintrag öffnenMysildecard · 4.8 · MedDRA system organ class (V.14.0) Adverse reaction Infections and infestations Common cellulitis, influenza,
Eintrag öffnenMysildecard · 4.8 · Of the 234 paediatric subjects treated in the short-term, placebo-controlled study, 220 subjects entered the l
Eintrag öffnenMysildecard · 4.8 · Paediatric population
Eintrag öffnenMysildecard · 4.8 · Reporting of suspected adverse reactions
Eintrag öffnenMysildecard · 4.8 · Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows con
Eintrag öffnenMysildecard · 4.8 · Reports from post-marketing experience are included in italics.
Eintrag öffnenMysildecard · 4.8 · Serious adverse events were reported in 94 (41%) of the 229 subjects receiving sildenafil. Of the 94 subjects
Eintrag öffnenMysildecard · 4.8 · Summary of the safety profile
Eintrag öffnenMysildecard · 4.8 · Tabulated list of adverse reactions
Eintrag öffnenMysildecard · 4.8 · The adverse reactions profile seen in this paediatric study was generally consistent with that in adults (see
Eintrag öffnenMysildecard · 4.8 · The following serious adverse events were considered to be treatment related, enterocolitis, convulsion, hyper
Eintrag öffnenMysildecard · 4.8 · The most common adverse reactions reported across the duration of the short-term and long-term studies were ge
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