Search results

• Halothane
  | metabolism = [[Liver|Hepatic]] ([[CYP2E1]]<ref>[http://redpoll.pharmacy.ualberta.ca/dr ...ly, halothane is not an [[ether]]. Attempts to find anaesthetics with less metabolism led to [[halogenated ethers]] such as [[enflurane]] and [[isoflurane]]. The
  6 KB (845 words) - 11:06, 20 September 2010
• Ivermectin
  | metabolism = liver; CYP450
  10 KB (1,292 words) - 16:41, 27 September 2010
• Quinine
  | metabolism = [[Liver|Hepatic]] (mostly [[CYP3A4]] and [[CYP2C19]]-mediated)
  27 KB (3,844 words) - 16:41, 27 September 2010
• Mefloquine
  | metabolism = Extensively hepatic; main metabolite is inactive
  13 KB (1,807 words) - 16:41, 27 September 2010
• Glibenclamide
  | metabolism = [[Liver|Hepatic]] [[hydroxylation]] ([[CYP2C9]]-mediated)
  6 KB (743 words) - 21:12, 31 August 2010
• Spectinomycin
  | metabolism =
  3 KB (327 words) - 16:41, 27 September 2010
• Bupivacaine
  | metabolism = [[hepatic]]
  6 KB (809 words) - 15:05, 6 July 2010
• Lidocaine
  | metabolism = [[Liver|Hepatic]], 90% [[CYP1A2]]-mediated
  15 KB (2,006 words) - 16:41, 27 September 2010
• Allopurinol
  | metabolism = hepatic (80% oxypurinol, 10% allopurinol ribosides) ...resulting in the production of [[uric acid]], the product of human purine metabolism.<ref name="pmid16507884"/> In addition to blocking uric acid production, in
  7 KB (864 words) - 16:41, 27 September 2010
• Chloroquine
  | metabolism = Liver ...s, which the parasite requires to construct its own protein and for energy metabolism. Digestion is carried out in a vacuole of the parasite cell.
  16 KB (2,187 words) - 16:41, 27 September 2010
• Chlorphenamine
  | metabolism = [[Liver|Hepatic]] ([[CYP2D6]])
  6 KB (745 words) - 15:05, 6 July 2010
• Dexamethasone
  | metabolism = [[hepatic]]
  18 KB (2,498 words) - 16:41, 27 September 2010
• Prednisolone
  | metabolism =
  7 KB (872 words) - 16:41, 27 September 2010
• Acetylcysteine
  | metabolism = [[hepatic]] ...ism is through scavenging of [[acetaldehyde]], a toxic intermediate in the metabolism of ethanol.<ref>Fawkes, SW [http://www.ceri.com/alcohol.htm CERI: Living wi
  28 KB (3,682 words) - 16:42, 27 September 2010
• Deferoxamine
  | metabolism = ?
  5 KB (714 words) - 20:14, 21 September 2010
• Naloxone
  | bioavailability = 2% (Oral, 90% absorption but high [[first-pass metabolism]]) | metabolism = [[Liver]]
  33 KB (4,541 words) - 10:57, 17 June 2016
• Penicillamine
  | metabolism = Hepatic * In [[Wilson's disease]], a rare genetic disorder of [[copper]] metabolism, penicillamine treatment relies on its binding to accumulated copper and el
  5 KB (570 words) - 20:14, 21 September 2010
• Carbamazepine
  | metabolism = [[Liver|Hepatic]]—by [[CYP3A4]], to active [[epoxide]] form (carbamazep ...channel blocker]]s.<ref name=Lexi-Comp/> Carbamazepine also increases the metabolism of the hormones in [[birth control pill]]s and can reduce their effectivene
  16 KB (2,164 words) - 16:42, 27 September 2010
• Phenobarbital
  | metabolism = [[Liver|Hepatic]] (mostly [[CYP2C19]]) Phenobarbital was used to treat [[neonatal jaundice]] by increasing liver metabolism and thus lowering [[bilirubin]] levels. In the 1950s, [[phototherapy]] was
  20 KB (2,657 words) - 16:42, 27 September 2010
• Phenytoin
  | metabolism = [[hepatic]]
  12 KB (1,686 words) - 16:42, 27 September 2010

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