Jump to content

Varenicline

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Paul gene (talk | contribs) at 01:26, 6 October 2008 (ISMP is a reliable secondary source. They used raw FDA numbers. FDA itself never conducted the analysis.). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Varenicline
Clinical data
License data
Routes of
administration
Oral
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Protein binding<20%
MetabolismLimited (<10%)
Elimination half-life24 hours
ExcretionRenal (81–92%)
Identifiers
  • 7,8,9,10-tetrahydro-6,10-methano-
    6H-pyrazino(2,3-h)(3)benzazepine
CAS Number
PubChem CID
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC13H13N3
Molar mass211.267 g/mol g·mol−1
3D model (JSmol)
  • C1C2CNCC1C3=CC4=NC=CN=
    C4C=C23

Varenicline (trade name Chantix in the USA and Champix in Europe and other countries, marketed by Pfizer, usually in the form of varenicline tartrate) is a prescription medication used to treat smoking addiction. Varenicline is a nicotinic receptor partial agonist. In this respect, it is similar to cytisine and different from nicotinic antagonist, bupropion, and nicotine replacement therapies (NRTs) like nicotine patches (commonly, "the patch") and nicotine gum. As a partial agonist, it both reduces cravings for and decreases the pleasurable effects of cigarettes and other tobacco products, and through these mechanisms it can assist some patients in stopping smoking.

Indications

Varenicline is indicated for (suggested for use in) smoking cessation. It is an alternative to NRTs and agonist medication and has demonstrated greater efficacy than them in comparable studies.[1]

The FDA has approved its use for twelve weeks. If smoking cessation has been achieved it may be continued for another twelve weeks.[2]

Varenicline has not been tested in children, those under 18 years old, or pregnant women, and therefore is not recommended for use by these groups. Women currently breastfeeding should also avoid this product, since varenicline may pass into the breast milk, leading to unknown effects on the child.

Mechanism of action

Varenicline is a partial agonist of the α4β2 subtype of the nicotinic acetylcholine receptor. In addition it acts on α3β4 and weakly on α3β2 and α6-containing receptors. A full agonism was displayed on α7-receptors.[3]

Pharmacokinetics

Most of the active compound is excreted renally (92-93%). A small proportion is glucuronidated, oxidated, N-formylated or conjugated to a hexose.[4] The elimination half-life is about 24 hours.

Side Effects

Nausea occurs commonly in people taking varenicline. Other less common side effects include headache, difficulty sleeping, and abnormal dreams. Rare side effects reported by people taking varenicline compared to placebo include change in taste, vomiting, abdominal pain, flatulence, and constipation.[5] In May 2008, Pfizer updated the safety information associated with Chantix, noting that "some patients have reported changes in behavior, agitation, depressed mood, suicidal thoughts or actions." [6]

In November 2007, the FDA announced it had received post-marketing reports that patients using Chantix for smoking cessation had experienced several serious symptoms, including suicidal ideation and occasional suicidal behavior, erratic behavior, and drowsiness. On February 1, 2008 the FDA issued an Alert to further clarify its findings, noting that "it appears increasingly likely that there is an association between Chantix and serious neuropsychiatric symptoms." It is unknown whether the psychiatric symptoms are related to the drug or to nicotine withdrawal symptoms, although not all patients had stopped smoking. The FDA is aware of the highly-publicized case of Carter Albrecht who, in an apparent state of delirium, was shot to death by his neighbour after hitting his girlfriend and then trying to forcibly enter the neighbor's house.[7] Although in this case the delirium appeared to be caused by taking varenicline with a high dose of alcohol, the FDA asked Pfizer for additional cases that might be similar. It also recommended that health care professionals and patients watch for behavioral and mood changes.[8]

Institute for Safe Medical Practices (ISMP) conducted an analysis of post-marketing adverse effects reports received by the FDA. According to this analysis, in the fourth quarter of 2007 varenicline accounted for more reports of serious side effects than any other drug. Suicidal acts and ideation, psychosis, and hostility or aggression, including homicidal ideation, were the most prominent psychiatric side effects. Multiple reports suggested that varenicline may be related to the loss of glycemic control and new onset of diabetes, heart rhythm disturbances, skin reactions, vision disturbances, seizures, abnormal muscle spasms and other movement disorders. However, ISMP warned that the reports do not establish that varenicline caused these side effects and only identify potential causes; most patients were taking multiple drugs; only a minority of side effects is usually reported so the large number of reports may not mean that varenicline is more dangerous than other drugs. ISMP concluded that further research and a priority review of the data by the FDA is necessary. [9]

On Thursday, May 22, 2008, The New York Times reported that the U.S. Federal Aviation Administration (F.A.A.) had announced the day before a ban on the use of Chantix (varenicline tartrate) for both pilots and air traffic controllers, due to concerns with possible adverse neuropsychiatric effects which could be detrimental to public safety.[10]

On Sunday, May 25, 2008, The Los Angeles Times reported that over 2 dozen traffic accidents had been linked to Chantix and reported to the FDA. Warnings had previously been issued by Pfizer regarding the risks of Chantix while driving, however these warnings have largely been ignored by doctors and patients.[11]

On Tuesday, June 17, 2008, The Washington Times reported on its Front Page that the United States Department of Veterans Affairs was testing Chantix on war veterans with Post Traumatic Stress Disorder without properly warning them of the side effects, and that in one case a veteran was almost killed when he had a psychotic episode and threatened police officers.[12]

History

Varenicline was discovered at Pfizer through the research aimed at modifying the structure of cytisine,[13] a European smoking cessation aid and also a partial α4β2-nicotinic antagonist.[14][15]

Varenicline received a "priority review" by the U.S. Food and Drug Administration in February 2006, shortening the usual 10-month review period to 6 months because of its demonstrated effectiveness in clinical trials and perceived lack of safety issues.[16] The agency's approval of the drug came on May 11, 2006.[2] Beginning August 1, 2006, varenicline has been available for sale in the United States, and on September 29, 2006, it was approved for sale in the European Union.

Footnotes

  1. ^ Jorenby D E, Hays J T, Rigotti N A, Azoulay S, Watsky E J, Williams K E, Billing C B, Gong J, Reeves K R (2006). "Efficacy of varenicline, an alpha4beta2 nicotinic acetylcholine receptor partial agonist, vs placebo or sustained-release bupropion for smoking cessation: a randomized controlled trial". JAMA. 296 (1): 56–63. doi:10.1001/jama.296.1.56. PMID 16820547.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^ a b U.S. Food and Drug Administration. FDA Approves Novel Medication for Smoking Cessation. Press release, 11 May 2006.
  3. ^ Mihalak KB, Carroll FI, Luetje CW (2006). "Varenicline is a partial agonist at alpha4beta2 and a full agonist at alpha7 neuronal nicotinic receptors". Mol. Pharmacol. 70 (3): 801–5. doi:10.1124/mol.106.025130. PMID 16766716.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ Obach RS, Reed-Hagen AE, Krueger SS, Obach BJ, O'Connell TN, Zandi KS, Miller S, Coe JW. Metabolism and disposition of varenicline, a selective alpha4beta2 acetylcholine receptor partial agonist, in vivo and in vitro. Drug Metab Dispos 2006;34:121-30. PMID 16221753.
  5. ^ American Cancer Society. "Cancer Drug Guide: Varenicline". Retrieved 2008-01-19.
  6. ^ "Important Information about Chantix". Retrieved 2008-05. {{cite web}}: Check date values in: |accessdate= (help)
  7. ^ "ABC News: Did Quit-Smoking Pill Lead to Man's Death?". Retrieved 2007-12-15. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  8. ^ "Early Communication About an Ongoing Safety Review: Varenicline (marketed as Chantix)". United States Food and Drug Administration. 2007. Retrieved 2007-11-21. {{cite web}}: Unknown parameter |month= ignored (help)
  9. ^ Institute for Safe Medical Practices. "Strong Safety Signal Seen for New Varenicline Risks". Retrieved 2008-05-21.
  10. ^ Saul, Stephanie (2008-05-22). "F.A.A. Bans Antismoking Drug, Citing Side Effects". New York Times. Retrieved 2008-05-22.
  11. ^ Alonso-Zaldivar, Ricardo (2008-05-25). "Drug taken to stop smoking is linked to traffic mishaps". Los Angeles Times. Retrieved 2008-05-25.
  12. ^ Hudson, Audrey (2008-06-17). "VA Testing Drugs on War Veterans". The Washington Times. p. A1.
  13. ^ Coe JW, Brooks PR, Vetelino MG; et al. (2005). "Varenicline: an alpha4beta2 nicotinic receptor partial agonist for smoking cessation". J. Med. Chem. 48 (10): 3474–7. doi:10.1021/jm050069n. PMID 15887955. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  14. ^ Schwartz JL (1979). "Review and evaluation of methods of smoking cessation, 1969-77. Summary of a monograph". Public Health Rep. 94 (6): 558–63. PMID 515342. PMC 1431736
  15. ^ Etter JF (2006). "Cytisine for smoking cessation: a literature review and a meta-analysis". Arch. Intern. Med. 166 (15): 1553–9. doi:10.1001/archinte.166.15.1553. PMID 16908787.
  16. ^ Kuehn BM (2006). "FDA speeds smoking cessation drug review". JAMA. 295 (6): 614. doi:10.1001/jama.295.6.614. PMID 16467225.

Template:Parasympathomimetics