Examples of using Lapatinib in English and their translations into Polish
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The following adverse reactions have been reported to have a causal association with lapatinib alone or lapatinib in combination with capecitabine,
A total of 991 patients were randomised to trastuzumab emtansine or lapatinib plus capecitabine as follows.
Co-administration of lapatinib with intravenously administered docetaxel did not significantly affect the AUC
Dosing of lapatinib one hour after a meal results in approximately 2-3 times higher systemic exposure, compared to dosing one hour before a meal see sections 4.5 and 5.2.
The combination of lapatinib and trastuzumab may offer complementary mechanisms of action as well as possible non-overlapping mechanisms of resistance.
Lapatinib treatment should only be initiated by a physician experienced in the administration of anti- cancer agents.
Diarrhoea, including severe diarrhoea, has been reported with lapatinib treatment see section 4.8.
Lapatinib pharmacokinetics have not been specifically studied in patients with renal impairment
Approximately 70 patients from study EGF114299 who have been randomised to the lapatinib+ AI arm with an exposure of approximately 6 months.
trastuzumab did not meaningfully alter the pharmacokinetics of these medicinal products(or the metabolites of capecitabine) or lapatinib.
1 indicates a lower risk with letrozole 2.5 mg+ lapatinib 1500 mg compared with letrozole 2.5 mg+ placebo.
Lapatinib has been associated with reports of decreases in LVEF see section 4.8.
Patients treated with Kadcyla also survived for 31 months compared with 25 months for patients treated with capecitabine and lapatinib.
Pre-treatment with a proton pump inhibitor(esomeprazole) decreased lapatinib exposure by an average of 27% range: 6% to 49.
The median duration of overall survival was 29.9 months in the trastuzumab emtansine arm compared with 25.9 months in the lapatinib plus capecitabine arm.
Tyverb should not be used in people who may be hypersensitive(allergic) to lapatinib or any of the other ingredients.
Lapatinib should be discontinued if changes in liver function are severe and patients should not be retreated see section 4.4.
Lapatinib has been associated with reports of decreases in left ventricular ejection fraction(LVEF) see section 4.8.
Concomitant treatment with substances that increase gastric pH should be avoided, as lapatinib solubility and absorption may decrease see section 4.5.
Concomitant treatment with substances that increase gastric pH should be avoided, as lapatinib solubility and absorption may decrease.