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metabolat normeperidine
normeperidine metabolite

metabolat 14-oh clarithromycin
oh clarithromycin metabolite

cefuroxime ma jkunx metabolat.
cefuroxime is not metabolised.

testosterone hu metabolat għal diversi
testosterone is metabolised to various

metabolat 25-o-desacetyl rifabutin
25-o-desacetyl rifabutin metabolite

testosterone hu metabolat primarjament fil-fwied.
testosterone is metabolised primarily in the liver.

telmisartan hu metabolat permezz ta’ konjugazzjoni għal glucuronide.
telmisartan is metabolised by conjugation to the glucuronide of the parent compound.

rilpivirine hydrochloride jiġi metabolat u eliminat primarjament mill-fwied.
rilpivirine hydrochloride is primarily metabolised and eliminated by the liver.

deferiprone hu metabolat l-aktar għall-konjugat glucuronide.
deferiprone is metabolised predominantly to a glucuronide conjugate.

biotrasformazzjoni deferiprone hu metabolat l- aktar għall- konjugat glucuronide.
biotransformation deferiprone is metabolised predominantly to a glucuronide conjugate.

telmisartan hu metabolat permezz ta’ konjugazzjoni għal glucuronide tal-kompost prinċipali.
telmisartan is metabolised by conjugation to the glucuronide of the parent compound.

meloxicam huwa metabolat għal alkoħol, derivattiv ta’ l-aċidu u għal diversi metaboliti polari.
meloxicam is metabolised to an alcohol, an acid derivative and to several polar metabolites.

testosterone hu metabolat għal diversi 17- ketosteroids u metaboliżmu addizzjonali jirriżulta fi glucuronides inattivi u konjugati oħrajn.
testosterone is metabolised to various 17-ketosteroids and further metabolism results in inactive glucuronides and other conjugates.

meloxicam huwa metabolat f’alkoħol, derivattiv ta’ l-aċidu u f’diversi metaboliti polari.
meloxicam is metabolised to an alcohol, an acid derivative and to several polar metabolites.

bl-istess mod, billi deferiprone hu metabolat fil-fwied, għandha tingħata attenzjoni f’pazjenti b’disfunzjoni epatika.
similarly, as deferiprone is metabolised in the liver, caution must be exercised in patients with hepatic dysfunction.

ziconotide hu peptide li jikkonsisti minn 25 amino acids li jseħħu b’mod naturali li għandhom konfigurazzjoni l, u ma jidhirx li hu metabolat b’mod apprezzabbli fis-csf.
ziconotide is a peptide consisting of 25 naturally-occurring amino acids of the l-configuration, and does not appear to be appreciably metabolised in the csf.

l-auc fiss ta’ tolterodine (2 mg darbtejn kuljum) tiżdied b’71% meta jingħata flimkien ma’ duloxetine (40 mg darbtejn kuljum), iżda ma jaffettwax il-farmakokinetika tal-metabolat attiv tiegħu 5-hydroxyl u mhux irrakkomandat li jsir aġġustament ta’ doża.
the co-administration of duloxetine (40 mg twice daily) increases steady state auc of tolterodine (2 mg twice daily) by 71 %, but does not affect the pharmacokinetics of its active 5- hydroxyl metabolite and no dosage adjustment is recommended.