Examples of using Tarceva in English and their translations into Danish
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Based on the results of pharmacokinetic studies, current smokers should be advised to stop smoking while taking Tarceva, as plasma concentrations could be reduced otherwise.
The median PFS was 9.7 weeks in the Tarceva group(95% CI,
Co-administration of rifampicin with a single 450 mg dose of Tarceva resulted in a mean erlotinib exposure(AUC) of 57.5% of that after a single 150 mg Tarceva dose in the absence of rifampicin treatment.
Current smokers, pharmacokinetic analyses at steady-state indicated a dose proportional increase in erlotinib exposure when the Tarceva dose was increased from 150 mg to the maximum tolerated dose of 300 mg.
in at least 10% of patients in the Tarceva group, are summarised by National Cancer Institute-Common Toxicity Criteria(NCI-CTC) Grade in Table 1.
other predisposing conditions including advanced age), Tarceva therapy should be interrupted and appropriate measures should be taken to intensively rehydrate the patients intravenously.
What is the risk associated with Tarceva?
Your doctor may decide to permanently stop your treatment with Tarceva.
This helps Tarceva stop the cancer cells from growing and multiplying.
Use of Tarceva in patients with severe renal impairment is not recommended.
Tarceva 25 mg One film-coated tablet contains 25 mg erlotinib as erlotinib hydrochloride.
Tarceva is available in strengths of 25 mg,
In case of suspected overdose, Tarceva should be withheld and symptomatic treatment initiated.
Your doctor might avoid treating you with these medicines while you are receiving Tarceva.
When prescribing Tarceva, factors associated with prolonged survival should be taken into account.
Tarceva is taken at least one hour before
Tarceva is available in strengths of 25 mg,
Tarceva is not recommended for use in patients with severe liver or kidney disease.
have been reported during use of Tarceva.
Tarceva must be taken at least 2 hours before or 10 hours after ranitidine dosing.