Examples of using Telithromycin in English and their translations into Swedish
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Ketek 400 mg film-coated tablets Telithromycin.
Its principal circulating metabolite represents approximately 13% of telithromycin AUC, and has little antimicrobial activity compared with the parent medicinal product.
magnesium hydroxide has no clinically relevant influence on telithromycin pharmacokinetics.
Antibiotics for infections called clarithromycin or telithromycin medicines for HIV called atazanavir,
If telithromycin treatment is deemed necessary, these patients may be treated with alternating daily
Quetiapine due to an increased risk of toxicity telithromycin and clarithromycin in patients with severe renal impairment due to an increased risk of hepatotoxicity
In subjects over 65(median 75 years), the maximum plasma concentration and AUC of telithromycin were increased approximately 2-fold compared with those achieved in young healthy adults.
The pharmacological action of telithromycin involves inhibition of bacterial protein synthesis
Sirolimus Due to its CYP3A4 inhibitory potential, telithromycin can increase blood concentrations of these CYP34A4 substrates.
When initiating telithromycin in patients already receiving any of theses immunosuppressive agents,
When telithromycin is discontinued, cyclosporin, tacrolimus
voriconazole);• antibiotics used to treat bacterial infections(telithromycin, rifampicin);• medicine used to treat HIV infection
covered by the antibacterial spectrum of telithromycin(see sections 4.4 and 5.1).
liver problems, Ketek should not be used with some medicines that may affect the way that telithromycin is broken down, including protease inhibitors(used in HIV infection) and ketoconazole an antifungal medicine.
such as clarithromycin or telithromycin see beginning of section 2 under‘Do not take Spedra.
covered by the antibacterial spectrum of telithromycin see sections 4.4 and 5.1.
Telithromycin displays moderate non-linear pharmacokinetics.
Telithromycin is widely distributed no.
Telithromycin is also a P-glycoprotein inhibitor.
Telithromycin is metabolised primarily by the liver.