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Celsentri · 4.8 · Description of selected adverse reactions
Eintrag öffnenCelsentri · 4.8 · Description of selected adverse reactions
Eintrag öffnenCelsentri · 4.8 · In HIV infected patients with severe immune deficiency at the time of initiation of combination antiretroviral
Eintrag öffnenCelsentri · 4.8 · In HIV infected patients with severe immune deficiency at the time of initiation of combination antiretroviral
Eintrag öffnenCelsentri · 4.8 · In treatment-naïve patients, the incidence of grade 3 and 4 laboratory abnormalities using ACTG criteria was s
Eintrag öffnenCelsentri · 4.8 · In treatment-naïve patients, the incidence of grade 3 and 4 laboratory abnormalities using ACTG criteria was s
Eintrag öffnenCelsentri · 4.8 · Laboratory abnormalities
Eintrag öffnenCelsentri · 4.8 · Laboratory abnormalities
Eintrag öffnenCelsentri · 4.8 · Maraviroc 300 mg Placebo + OBT Laboratory parameter Limit twice daily + OBT N =207* N =421* (%) (%) Hepatobili
Eintrag öffnenCelsentri · 4.8 · Maraviroc 300 mg Placebo + OBT Laboratory parameter Limit twice daily + OBT N =207* N =421* (%) (%) Hepatobili
Eintrag öffnenCelsentri · 4.8 · Paediatric population
Eintrag öffnenCelsentri · 4.8 · Paediatric population
Eintrag öffnenCelsentri · 4.8 · Reporting of suspected adverse reactions 42 Reporting suspected adverse reactions after authorisation of the m
Eintrag öffnenCelsentri · 4.8 · Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows con
Eintrag öffnenCelsentri · 4.8 · Summary of the safety profile
Eintrag öffnenCelsentri · 4.8 · Summary of the safety profile
Eintrag öffnenCelsentri · 4.8 · System Organ Class Adverse reaction Frequency Infections and infestations Pneumonia, oesophageal candidiasis u
Eintrag öffnenCelsentri · 4.8 · System Organ Class Adverse reaction Frequency Infections and infestations Pneumonia, oesophageal candidiasis u
Eintrag öffnenCelsentri · 4.8 · Table 3: Adverse reactions observed in clinical trials or post-marketing
Eintrag öffnenCelsentri · 4.8 · Table 3: Adverse reactions observed in clinical trials or post-marketing
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