Voorbeelden van het gebruik van Sunitinib in het Engels en hun vertalingen in het Nederlands
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The pharmacokinetics of sunitinib were evaluated in 135 healthy volunteers
Steady-state concentrations of sunitinib and its primary active metabolite are achieved within 10 to 14 days.
Sunitinib did not induce structural chromosome aberrations in human peripheral blood lymphocyte cells in vitro.
It is not known whether sunitinib or its primary active metabolite is excreted in human milk.
sorafenib, sunitinib.
At approximately twice therapeutic concentrations, sunitinib has been shown to prolong the QTcF Interval Frederica's Correction.
During sunitinib treatment, routine monitoring of thyroid function should be performed every 3 months.
A hazard ratio favouring sunitinib was observed in all subgroups of baseline characteristics evaluated,
No starting dose adjustment is recommended when administering sunitinib to patients with mild
No starting dose adjustment is required when administering sunitinib to patients with renal impairment(mild-severe)
All patients should be observed closely for signs and symptoms of thyroid dysfunction on sunitinib treatment.
The safety of continued sunitinib treatment in patients with moderate to severe proteinuria has not been systematically evaluated.
symptoms of hepatic failure are present, sunitinib should be discontinued
Therefore, the decision to resume sunitinib therapy following a major surgical intervention should be based upon clinical judgment of recovery from surgery.
Sunitinib therapy should be discontinued in patients who develop necrotising fasciitis,
Sunitinib treatment may be associated with cholecystitis,
Use sunitinib with caution in patients who are at risk for,
Temporary suspension of sunitinib is recommended;
The infections observed most commonly with sunitinib treatment are infections typically seen in cancer patients,
If angioedema due to hypersensitivity occurs, sunitinib treatment should be interrupted and standard medical care provided.