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{{Drugbox|
{{Drugbox| verifiedrevid = 306701498
|
|IUPAC_name = 2-([3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl]methylsulfinyl)-1''H''-benzo[''d'']imidazole
|IUPAC_name = 2-([3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl]methylsulfinyl)-1''H''-benzo[''d'']imidazole
| image=Lansoprazole.svg
| image=Lansoprazole.svg
| image2 = Lansoprazole 3D.png
| image2 = Lansoprazole 3D.png
| width = 250px
| width = 250px
| CASNo_Ref = {{cascite}}
| CAS_number=103577-45-3
| CAS_number=103577-45-3
| ChemSpiderID = 3746
| ChemSpiderID = 3746

Revision as of 16:22, 12 September 2009

Lansoprazole
Clinical data
License data
Pregnancy
category
  • AU: B3
Routes of
administration
Oral, IV
ATC code
Legal status
Legal status
  • US: WARNING[1]
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability80% or more
Protein binding97%
MetabolismHepatic (CYP3A4- and CYP2C19-mediated)
Elimination half-life1–1.5 hours
ExcretionRenal and fecal
Identifiers
  • 2-([3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl]methylsulfinyl)-1H-benzo[d]imidazole
CAS Number
PubChem CID
DrugBank
ChemSpider
CompTox Dashboard (EPA)
ECHA InfoCard100.173.220 Edit this at Wikidata
Chemical and physical data
FormulaC16H14F3N3O2S
Molar mass369.363 g/mol g·mol−1
3D model (JSmol)
  • O=S(Cc1nccc(OCC(F)(F)F)c1C)c1nc2ccccc2[nH]1
  (verify)

Lansoprazole (lan-SOE-pra-zole, INN) is a proton pump inhibitor which prevents the stomach from producing acid. It is manufactured by a number of companies worldwide under several brand names (some brand names include: Prevacid, Helicid, Zoton, Inhibitol). It was first approved by the FDA in 1995.[2]

Pharmacology

Lansoprazole is a proton pump inhibitor (PPI) in the same pharmacologic class as omeprazole. Lansoprazole has been marketed for many years and is one of several PPIs available.[3]

Lansoprazole's plasma elimination half-life is not proportional to the duration of the drug's effects (i.e. gastric acid suppression). The mean plasma elimination half-life is 1.5 hours,[4] and the effects of the drug last for over 24 hours after it has been used for 1 day or more.[citation needed]

Indications

Lansoprazole is indicated for:

Drug Interactions

Side effects

Proton pump inhibitors may be associated with a greater risk of hip fractures,[5] clostridium difficile-associated diarrhea.[6] Patients are frequently administered the drugs in intensive care as a protective measure against ulcers, but this use is also associated with a 30% increase in occurrence of pneumonia.[7]

Brand names

Prevacid 30 mg

The drug is sold under several brand names, including: [2]

  • Agopton (Germany)
  • Aprazol (Turkey)
  • Digest (Indonesia)
  • Duogast (Syria)
  • Lanpro (India)
  • Lanzol (India)
  • Lanzul (Slovenia)
  • Lansoptol (Hungary)
  • Lansox (Italy)
  • Lansoloc (South Africa)
  • Lanton (Israel)
  • Lanzor (France)
  • Laprazol (Greece)
  • Limpidex (Italy)
  • Monolitum (Spain)
  • Ogast and OgastORO (France)
  • Ogastro (Mexico)
  • Prevacid (U.S. and Canada) Prevacid is a product of Takeda Pharmaceuticals.
  • pro-ulco (Spain)
  • Prosogan and Prosogan FD (Indonesia)
  • Refluxon (Hungary)
  • SOLOX (New Zealand)
  • Takepron (Japan)
  • Zoton (Italy, Ireland, Australia, UK)
  • ZOMEL (Ireland)

Lansoprazole is also available as a generic drug in the UK, Canada, Belgium, France, Colombia, Italy and Mexico.

References

  1. ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.
  2. ^ a b Mosby's Drug Consult: Lansoprazole
  3. ^ http://www.patient.co.uk/showdoc/30002943/
  4. ^ a b "Prevacid Pharmacology, Pharmacokinetics, Studies, Metabolism". RxList.com. 2007. Retrieved 2007-04-14. Cite error: The named reference "RxList" was defined multiple times with different content (see the help page).
  5. ^ Yang YX, Lewis JD, Epstein S, Metz DC (2006). "Long-term Proton Pump Inhibitor Therapy and Risk of Hip Fracture". JAMA. 296 (24): 2947–53. doi:10.1001/jama.296.24.2947. PMID 17190895.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. ^ "Proton pump inhibitors and Clostridium difficile". Bandolier. 2003. Retrieved 2007-07-13.
  7. ^ Shoshana J. Herzig, MD; Michael D. Howell, MD, MPH; Long H. Ngo, PhD; Edward R. Marcantonio, MD, SM (2009). "Acid-Suppressive Medication Use and the Risk for Hospital-Acquired Pneumonia=JAMA". JAMA the Journal of the American Medical Association. 301 (20): 2120–2128. doi:10.1001/jama.2009.722. PMID 19470989.{{cite journal}}: CS1 maint: multiple names: authors list (link)

External links

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