Varenicline
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| Trade names | Champix, Chantix, others |
AHFS/Drugs.com | Monograph |
| MedlinePlus | a606024 |
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| Routes of administration | By mouth |
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| Protein binding | <20% |
| Metabolism | Limited (<10%) |
| Elimination half-life | 24 hours |
| Excretion | Renal (81–92%) |
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| Formula | C13H13N3 |
| Molar mass | 211.267 g/mol |
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Varenicline (trade name Chantix and Champix), is a prescription medication used to treat nicotine addiction. It reduces both craving for and decreases the pleasurable effects of cigarettes and other tobacco products.
It is a high-affinity partial agonist for the α4β2 nicotinic acetylcholine receptor subtype (nACH) that leads to the release of dopamine in the nucleus accumbens when activated, and therefore, has the capacity to reduce the feelings of craving and withdrawal caused by smoking cessation.[1] In this respect it is similar to cytisine and different from the nicotinic antagonist bupropion and nicotine replacement therapies (NRTs) like nicotine patches and nicotine gum.
Contents
1 Medical uses
2 Side effects
2.1 Depression and suicide
2.2 Cardiovascular disease
2.3 Alcohol
3 Mechanism of action
4 Pharmacokinetics
5 History
6 See also
7 References
8 External links
Medical uses
Varenicline is used for smoking cessation. A meta-analysis found that less than 20% of people treated with vareniciline remain abstinent from smoking at one year.[2] In a 2009 meta-analysis varenicline was found to be more effective than bupropion (odds ratio 1.40) and NRTs (odds ratio 1.56).[3]
A 2013 Cochrane overview and network meta-analysis concluded that varenicline is the most effective medication for tobacco cessation and that smokers were nearly three times more likely to quit on varenicline than with placebo treatment. Varenicline was more efficacious than bupropion or NRT and as effective as combination NRT for tobacco smoking cessation.[4][5]
The United States' Food and Drug Administration (US FDA) has approved the use of varenicline for up to twelve weeks. If smoking cessation has been achieved it may be continued for another twelve weeks.[6]
Varenicline has not been tested in those under 18 years old or pregnant women and therefore is not recommended for use by these groups.[7] Varenicline is considered a class C pregnancy drug, as animal studies have shown no increased risk of congenital anomalies, however, no data from human studies is available.[8] An observational study is currently being conducted assessing for malformations related to varenicline exposure, but has no results yet.[9] An alternate drug is preferred for smoking cessation during breastfeeding due to lack of information and based on the animal studies on nicotine.[10]
Side effects
Mild nausea is the most common side effect and is seen in approximately 30% of people taking varenicline though this rarely (<3%) results in discontinuation of the medication.[5] Other less common side effects include headache, difficulty sleeping, and nightmares. Rare side effects reported by people taking varenicline compared to placebo include change in taste, vomiting, abdominal pain, flatulence, and constipation. It has been estimated that for every five subjects taking varenicline at maintenance doses, there will be an event of nausea, and for every 24 and 35 treated subjects, there will be an event of constipation and flatulence respectively. Gastrointestinal side-effects lead to discontinuation of the drug in 2% to 8% of people using varenicline.[11][12] Incidence of nausea is dose-dependent: incidence of nausea was higher in people taking a larger dose (30%) versus placebo (10%) as compared to people taking a smaller dose (16%) versus placebo (11%).[13]
Depression and suicide
In 2007, the US FDA had announced it had received post-marketing reports of thoughts of suicide and occasional suicidal behavior, erratic behavior, and drowsiness among people using varenicline for smoking cessation. In 2009, the US FDA required varenicline to carry a boxed warning that the drug should be stopped if any of these symptoms are experienced.[14]
A 2014 systematic review did not find evidence of an increased suicide risk.[15] Other analyses have reached the same conclusion and found no increased risk of neuropsychiatric side effects with varenicline.[4][5] No evidence for increased risks of cardiovascular events, depression, or self-harm with varenicline versus nicotine replacement therapy has been found in one post-marketing surveillance study.[16]
In 2016 the FDA removed the black box warning.[17] People are still advised to stop the medication if they "notice any side effects on mood, behavior, or thinking."[17][18][19]
Cardiovascular disease
In June 2011, the US FDA issued a safety announcement that varenicline may be associated with "a small, increased risk of certain cardiovascular adverse events in people who have cardiovascular disease."[20]
A prior 2011 review had found increased risk of cardiovascular events compared with placebo.[21] Expert commentary in the same journal raised doubts about the methodology of the review,[22][23] concerns which were echoed by the European Medicines Agency and subsequent reviews.[24][25] Of specific concern were "the low number of events seen, the types of events counted, the higher drop-out rate in people receiving placebo, the lack of information on the timing of events, and the exclusion of studies in which no-one had an event."
In contrast, multiple recent systematic reviews and meta-analyses have found no increase in overall or serious adverse cardiovascular events (including for individuals at risk of developing cardiovascular disease) associated with varenicline use.[25][26][27][28]
Alcohol
It is recommended that people reduce the amount of alcohol they drink.[29]
Mechanism of action
Varenicline displays full agonism on α7 nicotinic acetylcholine receptors and is a partial agonist on the α4β2, α3β4, and α6β2 subtypes.[30][31][32] In addition, it is a weak agonist on the α3β2 containing receptors.
Varenicline's partial agonism on the α4β2 receptors rather than nicotine's full agonism produces less effect of dopamine release than nicotine's. This α4β2 competitive binding reduces the ability of nicotine to bind and stimulate the mesolimbic dopamine system - similar to the method of action of buprenorphine in the treatment of opioid addiction.[5]
Pharmacokinetics
Most of the active compound is excreted by the kidneys (92–93%). A small proportion is glucuronidated, oxidised, N-formylated or conjugated to a hexose.[33] The elimination half-life is about 24 hours.
History
Use of Cytisus plant as a smoking substitute during World War II[34] led to use as a cessation aid in eastern Europe and extraction of cytisine.[35]Cytisine analogs led to varenicline at Pfizer.[36][37][38]
Varenicline received a "priority review" by the US FDA 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.[39] The agency's approval of the drug came on May 11, 2006.[6] On August 1, 2006, varenicline was made available for sale in the United States and on September 29, 2006, was approved for sale in the European Union.[40]
See also
- Nicotinic agonist
References
^ Tashkin DP (August 2015). "Smoking Cessation in Chronic Obstructive Pulmonary Disease". Seminars in Respiratory and Critical Care Medicine. 36 (4): 491–507. doi:10.1055/s-0035-1555610. PMID 26238637..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
^ Rosen LJ, Galili T, Kott J, Goodman M, Freedman LS (May 2018). "Diminishing benefit of smoking cessation medications during the first year: a meta-analysis of randomized controlled trials". Addiction. 113 (5): 805–816. doi:10.1111/add.14134. PMC 5947828. PMID 29377409.
^ Mills EJ, Wu P, Spurden D, Ebbert JO, Wilson K (September 2009). "Efficacy of pharmacotherapies for short-term smoking abstinance: a systematic review and meta-analysis". Harm Reduction Journal. 6: 25. doi:10.1186/1477-7517-6-25. PMC 2760513. PMID 19761618.
^ ab Cahill K, Stevens S, Perera R, Lancaster T (May 2013). "Pharmacological interventions for smoking cessation: an overview and network meta-analysis". The Cochrane Database of Systematic Reviews (Systematic Review & Meta-Analysis). 5 (5): CD009329. doi:10.1002/14651858.CD009329.pub2. PMID 23728690.
^ abcd Elrashidi MY, Ebbert JO (June 2014). "Emerging drugs for the treatment of tobacco dependence: 2014 update". Expert Opinion on Emerging Drugs (Review). 19 (2): 243–60. doi:10.1517/14728214.2014.899580. PMID 24654737.
^ ab U.S. Food and Drug Administration.FDA Approves Novel Medication for Smoking Cessation. Press release, 11 May 2006.
^ Coleman T, Chamberlain C, Davey MA, Cooper SE, Leonardi-Bee J (December 2015). "Pharmacological interventions for promoting smoking cessation during pregnancy". The Cochrane Database of Systematic Reviews (12): CD010078. doi:10.1002/14651858.CD010078.pub2. PMID 26690977.
^ Cressman AM, Pupco A, Kim E, Koren G, Bozzo P (May 2012). "Smoking cessation therapy during pregnancy". Canadian Family Physician Medecin De Famille Canadien. 58 (5): 525–7. PMC 3352787. PMID 22586193.
^ Clinical trial number NCT01290445 for "Varenicline Pregnancy Cohort Study" at ClinicalTrials.gov
^ "LactMed". nih.gov.
^ Leung LK, Patafio FM, Rosser WW (September 2011). "Gastrointestinal adverse effects of varenicline at maintenance dose: a meta-analysis". BMC Clinical Pharmacology. 11 (1): 15. doi:10.1186/1472-6904-11-15. PMC 3192741. PMID 21955317.
^ American Cancer Society. "Cancer Drug Guide: Varenicline". Retrieved 2008-01-19.
^ "DailyMed - CHANTIX- varenicline tartrate". nih.gov.
^ FDA. "Public Health Advisory: FDA Requires New Boxed Warnings for the Smoking Cessation Drugs Chantix and Zyban". Retrieved 2009-07-01.
^ Hughes JR (January 2016). "Varenicline as a Cause of Suicidal Outcomes". Nicotine & Tobacco Research. 18 (1): 2–9. doi:10.1093/ntr/ntu275. PMID 25572451.
^ Kotz D, Viechtbauer W, Simpson C, van Schayck OC, West R, Sheikh A (October 2015). "Cardiovascular and neuropsychiatric risks of varenicline: a retrospective cohort study". The Lancet. Respiratory Medicine (retrospective cohort). 3 (10): 761–8. doi:10.1016/S2213-2600(15)00320-3. PMC 4593936. PMID 26355008.
^ ab Commissioner, Office of the. "Safety Alerts for Human Medical Products - Chantix (varenicline) and Zyban (bupropion): Drug Safety Communication - Mental Health Side Effects Revised". www.fda.gov. Retrieved 20 December 2016.
^ Palmer G, Massey V (May 1969). "Electron paramagnetic resonance and circular dichroism studies on milk xanthine oxidase". The Journal of Biological Chemistry. 244 (10): 2614–20. doi:10.1186/1753-6561-9-S1-A31. PMC 4306032.
^ Yeung E, Bachi B, Long B, Lee J, Chao Y (2015). "Varenicline and Depression: a Literature Review" (PDF). World Journal of Medical Education and Research. 9 (1): 24–29.
^ "FDA Drug Safety Communication: Chantix (varenicline) may increase the risk of certain cardiovascular adverse events in patients with cardiovascular disease". 2011-06-16.
^ Singh S, Loke YK, Spangler JG, Furberg CD (September 2011). "Risk of serious adverse cardiovascular events associated with varenicline: a systematic review and meta-analysis". CMAJ. 183 (12): 1359–66. doi:10.1503/cmaj.110218. PMC 3168618. PMID 21727225.
^ Takagi H, Umemoto T (September 2011). "Varenicline: quantifying the risk". CMAJ. 183 (12): 1404, author reply 1405, 1407. doi:10.1503/cmaj.111-2063. PMC 3168634. PMID 21896705.
^ Samuels L (September 2011). "Varenicline: cardiovascular safety". CMAJ. 183 (12): 1407–8, author reply 1408. doi:10.1503/cmaj.111-2073. PMC 3168639. PMID 21896709.
^ "European Medicine Agency confirms positive benefit-risk balance for Champix". 2011-07-21.
^ ab Prochaska JJ, Hilton JF (May 2012). "Risk of cardiovascular serious adverse events associated with varenicline use for tobacco cessation: systematic review and meta-analysis". BMJ (Systematic Review & Meta-Analysis). 344: e2856. doi:10.1136/bmj.e2856. PMC 3344735. PMID 22563098.
^ Mills EJ, Thorlund K, Eapen S, Wu P, Prochaska JJ (January 2014). "Cardiovascular events associated with smoking cessation pharmacotherapies: a network meta-analysis". Circulation (Network Meta-Analysis). 129 (1): 28–41. doi:10.1161/CIRCULATIONAHA.113.003961. PMC 4258065. PMID 24323793.
^ Pipe AL (October 2014). "Network meta-analysis demonstrates the safety of pharmacotherapy for smoking cessation in cardiovascular patients". Evidence-Based Medicine (Review & Commentary). 19 (5): 193. doi:10.1136/eb-2014-110030. PMID 24917603.
^ Rowland K (April 2014). "ACP Journal Club. Review: Nicotine replacement therapy increases CVD events; bupropion and varenicline do not". Annals of Internal Medicine (Review & Commentary). 160 (8): JC2. doi:10.7326/0003-4819-160-8-201404150-02002. PMID 24733219.
^ Research, Center for Drug Evaluation and. "Drug Safety and Availability - FDA Drug Safety Communication: FDA updates label for stop smoking drug Chantix (varenicline) to include potential alcohol interaction, rare risk of seizures, and studies of side effects on mood, behavior, or thinking". www.fda.gov.
^ Mihalak KB, Carroll FI, Luetje CW (September 2006). "Varenicline is a partial agonist at alpha4beta2 and a full agonist at alpha7 neuronal nicotinic receptors". Molecular Pharmacology. 70 (3): 801–5. doi:10.1124/mol.106.025130. PMID 16766716.
^ Mineur YS, Picciotto MR (December 2010). "Nicotine receptors and depression: revisiting and revising the cholinergic hypothesis". Trends in Pharmacological Sciences. 31 (12): 580–6. doi:10.1016/j.tips.2010.09.004. PMC 2991594. PMID 20965579.
^ Bordia T, Hrachova M, Chin M, McIntosh JM, Quik M (August 2012). "Varenicline is a potent partial agonist at α6β2* nicotinic acetylcholine receptors in rat and monkey striatum". The Journal of Pharmacology and Experimental Therapeutics. 342 (2): 327–34. doi:10.1124/jpet.112.194852. PMC 3400806. PMID 22550286.
^ Obach RS, Reed-Hagen AE, Krueger SS, Obach BJ, O'Connell TN, Zandi KS, Miller S, Coe JW (January 2006). "Metabolism and disposition of varenicline, a selective alpha4beta2 acetylcholine receptor partial agonist, in vivo and in vitro". Drug Metabolism and Disposition. 34 (1): 121–30. doi:10.1124/dmd.105.006767. PMID 16221753.
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^ Coe JW, Brooks PR, Vetelino MG, Wirtz MC, Arnold EP, Huang J, Sands SB, Davis TI, Lebel LA, Fox CB, Shrikhande A, Heym JH, Schaeffer E, Rollema H, Lu Y, Mansbach RS, Chambers LK, Rovetti CC, Schulz DW, Tingley FD, O'Neill BT (May 2005). "Varenicline: an alpha4beta2 nicotinic receptor partial agonist for smoking cessation". Journal of Medicinal Chemistry. 48 (10): 3474–7. doi:10.1021/jm050069n. PMID 15887955.
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^ European Medicines Agency (2011-01-28). "EPAR summary for the public. Champix varenicline". London. Retrieved 2011-02-14.
External links
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- Manufacturer's website USA
- Manufacturer's website UK
- FDA Alert
- Package insert
