Voorbeelden van het gebruik van Study with axitinib in het Engels en hun vertalingen in het Nederlands
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In a controlled clinical study with axitinib for the treatment of patients with RCC, liver-related events were reported.
In a controlled clinical study with axitinib for the treatment of patients with RCC, venous embolic
Hypertension In a controlled clinical study with axitinib for the treatment of patients with RCC,
In a controlled clinical study with axitinib for the treatment of patients with RCC, one patient inadvertently received a dose of 20 mg twice daily for 4 days and experienced dizziness Grade 1.
In a controlled clinical study with axitinib for the treatment of patients with RCC,
In a controlled clinical study with axitinib for the treatment of patients with RCC, polycythaemia was reported in 1.4% of patients receiving axitinib. .
In a controlled clinical study with axitinib for the treatment of patients with RCC, polycythaemia was reported as an adverse reaction in 0.3% of patients receiving axitinib. .
In a controlled clinical study with axitinib for the treatment of patients with RCC, hypothyroidism was reported in 20.9% of patients
In a controlled clinical study with axitinib for the treatment of patients with RCC, events of hypothyroidism
In a controlled clinical study with axitinib for the treatment of patients with RCC, venous embolic
In a controlled clinical study with axitinib for the treatment of patients with RCC, gastrointestinal perforation was reported in one patient(0.3%, all-causality incidence) receiving axitinib. .
In a controlled clinical study with axitinib for the treatment of patients with RCC, Grade 3/4 arterial embolic
In a controlled clinical study with axitinib for the treatment of patients with RCC that excluded patients with untreated brain metastasis, haemorrhagic adverse reactions were reported in 21.4% of patients receiving axitinib. .
In a controlled clinical study with axitinib for the treatment of patients with RCC that excluded patients with untreated brain metastasis, haemorrhagic adverse reactions were reported in 10.6% of patients receiving axitinib. .
In a controlled clinical study with axitinib for the treatment of patients with RCC, arterial embolic
In a controlled clinical study with axitinib(N 359) for the treatment of patients with RCC, cardiac failure events were reported in 1.7% patients receiving axitinib,
In clinical studies with axitinib for the treatment of patients with RCC, hypertension was very commonly reported see section 4.8.
In clinical studies with axitinib, events of gastrointestinal perforation
In clinical studies with axitinib, events of PRES were reported see section 4.8.
In clinical studies with axitinib, proteinuria, including that of Grade 3
In clinical studies with axitinib, proteinuria, including that of Grade 3 severity,
In clinical studies with axitinib for the treatment of patients with RCC, patients with serum creatinine>
In clinical studies with axitinib for the treatment of patients with RCC, events of hypothyroidism
In clinical studies with axitinib, arterial embolic
In clinical studies with axitinib, the systemic exposure to axitinib was approximately two-fold higher in subjects with moderate hepatic impairment(Child-Pugh class B)
In clinical studies with axitinib, venous embolic
In four clinical studies with axitinib for the treatment of patients with RCC(N 537),
In pooled clinical studies with axitinib(N 672) for the treatment of patients with RCC, arterial embolic
In pooled clinical studies with axitinib(N 672) for the treatment of patients with RCC,
In pooled clinical studies with axitinib(N 672) for the treatment of patients with RCC, haemorrhagic events were reported in 25.7% of patients receiving axitinib. .