Examples of using Lapatinib in English and their translations into Swedish
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Medicine
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Ecclesiastic
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Computer
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Lapatinib dosing should be discontinued if changes in liver function are severe and patients should not be retreated.
In vitro studies indicate that lapatinib is a substrate for the transporters BCRP(ABCG1)
Lapatinib pharmacokinetics have not been specifically studied in patients with renal impairment or in patients undergoing haemodialysis.
trastuzumab did not meaningfully alter the pharmacokinetics of these medicinal products(or the metabolites of capecitabine) or lapatinib.
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.
Lapatinib has been associated with reports of decreases in left ventricular ejection fraction(LVEF) see section 4.8.
trastuzumab did not meaningfully alter the pharmacokinetics of these agents(or the metabolites of capecitabine) or lapatinib.
In rats, growth retardation was observed in pups which were exposed to lapatinib via breast milk.
The patient and the adverse event profile of lapatinib should be borne in mind when considering the patient's ability to perform tasks that require judgement, motor or cognitive skills.
Lapatinib AUC values were approximately 3- and 4-fold higher(Cmax approximately 2.5
In patients who took up to 5000 mg of lapatinib, symptoms observed include known lapatinib associated events(see section 4.8)
Lapatinib AUC values were approximately 3-
these events were comparable in nature and severity to those reported from the lapatinib clinical programme see section 4.4- cardiac toxicity.
the incidence of cardiac events including LVEF decreases was higher(7%) versus the lapatinib alone arm(2%) in the pivotal trial.
Each film-coated tablet contains lapatinib ditosylate monohydrate, equivalent to 250 mg lapatinib.
It is not known whether lapatinib is excreted in human milk.
Lapatinib, due to increased hepatotoxicity of lapatinib likely due to induction of CYP3A4 metabolism.
Lapatinib did not significantly inhibit the following enzymes in human liver microsomes.
The half-life of lapatinib measured after single doses increases with increasing dose.