Alosetron

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Alosetron
Systematic (IUPAC) name
5-methyl-2-[(4-methyl-1H-imidazol-5-yl)methyl]-
3,4-dihydro-2H-pyrido[4,3-bindol-1(5H)-one
Identifiers
CAS number 122852-42-0
ATC code A03AE01
PubChem 2099
DrugBank APRD00580
Chemical data
Formula C17H18N4O 
Mol. mass 294.351 g/mol
Pharmacokinetic data
Bioavailability 50–60%
Protein binding 82%
Metabolism Hepatic (including CYP2C9, CYP3A4 and CYP1A2)
Half life 1.5–1.7 hours
Excretion Renal 73%, faecal 24%
Therapeutic considerations
Pregnancy cat.

B (U.S.)

Legal status

℞-only (U.S.)

Routes Oral

Alosetron is a 5-HT3 antagonist used for the management of severe diarrhoea-predominant irritable bowel syndrome (IBS) in women only. It was withdrawn from the market in 2000 owing to the occurrence of serious life-threatening gastrointestinal adverse effects, but was reintroduced in 2002 with availability and use restricted; it was the first drug ever returned to the U.S. market after withdrawal for safety concerns.[1] It is currently marketed by GlaxoSmithKline under the trade name Lotronex.

Contents

Mode of action

Alosetron, while being a 5-HT3 antagonist like ondansetron, is not an antiemetic. Alosetron has an antagonist action on the 5-HT3 receptors of the enteric nervous system of the gastrointestinal tract.

Serious adverse effects

Alosetron was withdrawn in 2000 following the association of alosetron with serious life-threatening gastrointestinal adverse effects. The cumulative incidence of ischaemic colitis was 2 in 1000, while serious complications arising from constipation (obstruction, perforation, impaction, toxic megacolon, secondary colonic ischaemia, death) was 1 in 1000.[2]

References

  1. ^ Pollack, A. "F.D.A. Panel Recommends M.S. Drug Despite Lethal Risk", The New York Times, 2006-03-09. Retrieved on 2008-03-13. 
  2. ^ GlaxoSmithKline plc. Lotronex (U.S. Prescribing Information). Brentford: GlaxoSmithKline; 2002.

See also

Wikipedia content modification information:

  • This page was last modified on 12 June 2008, at 22:36.

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