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Skeletal formula of colchicine
Ball-and-stick model of the colchicine molecule
Trade namesColcrys, Mitigare, others
  • N-[(7S)-1,2,3,10-Tetramethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl]acetamide
Clinical data
Main usesGout, Behçet's disease[1][2][3]
Side effectsGastrointestinal upset[4]
  • AU: D
  • US: C (Risk not ruled out)
Routes of
By mouth
Defined daily dose1 mg[5]
External links
License data
Legal status
Protein binding35-44%
MetabolismMetabolism, partly by CYP3A4
Elimination half-life26.6-31.2 hours
ExcretionFaeces (65%)
Chemical and physical data
Molar mass399.437 g·mol−1
3D model (JSmol)
  • O=C(N[C@@H]3C\1=C\C(=O)C(\OC)=C/C=C/1c2c(cc(OC)c(OC)c2OC)CC3)C
  • InChI=1S/C22H25NO6/c1-12(24)23-16-8-6-13-10-19(27-3)21(28-4)22(29-5)20(13)14-7-9-18(26-2)17(25)11-15(14)16/h7,9-11,16H,6,8H2,1-5H3,(H,23,24)/t16-/m0/s1 checkY

Colchicine is a medication used to treat gout and Behçet's disease.[1][2][3] In gout, it is less preferred to NSAIDs or steroids.[2] Other uses include the prevention of pericarditis and familial Mediterranean fever.[2][6] It is taken by mouth.[2]

Common side effects include gastrointestinal upset, particularly at high doses.[4] Severe side effects may include low blood cells and rhabdomyolysis.[2] Safety of use during pregnancy is unclear while use during breastfeeding appears safe.[2][7] Excessive doses may result in death.[2] Colchicine works by decreasing inflammation via multiple mechanisms.[8]

Colchicine, in the form of the autumn crocus, has been used as early as 1500 BC to treat joint swelling.[9] It was approved for medical use in the United States in 1961.[10] It is available as a generic medication.[7] In the United Kingdom, a month's supply costs the NHS about £7 as of 2019 while in Canada it is about 10 CAD as of 2021.[7][11] In the United States, the wholesale cost of this amount is about US$252.[12] In 2017, it was the 201st most commonly prescribed medication in the United States, with more than two million prescriptions.[13][14]

Medical uses


Colchicine is an alternative for those unable to tolerate NSAIDs in gout.[15] At high doses, side effects (primarily gastrointestinal upset) limit its use.[16][17] At lower doses, it is well tolerated.[16][18][19][20] One review found low-quality evidence that low-dose colchicine (1.8 mg in one hour or 1.2 mg per day) reduced gout symptoms and pain, whereas high-dose colchicine (4.8 mg over 6 hours) was effective against pain, but caused more severe side effects, such as diarrhea, nausea or vomiting.[19]

For treating gout symptoms, colchicine is used orally with or without food, as symptoms first appear.[21] Subsequent doses may be needed if symptoms worsen.[21][19] There is preliminary evidence that daily colchicine (0.6 mg twice daily) was effective as a long-term prophylaxis when used with allopurinol to reduce the risk of increased uric acid levels and acute gout flares,[22] although adverse gastrointestinal effects may occur.[23]

Other conditions

Colchicine is also used as an anti-inflammatory agent for long-term treatment of Behçet's disease.[24] It appears to have limited effect in relapsing polychondritis, as it may only be useful for the treatment of chondritis and mild skin symptoms.[25] It is a component of therapy for several other conditions, including pericarditis, pulmonary fibrosis, biliary cirrhosis, various vasculitides, pseudogout, spondyloarthropathies, calcinosis, scleroderma, and amyloidosis.[24][26][27] Research regarding the efficacy of colchicine in many of these diseases has not been performed.[27]

It is also used in the treatment of familial Mediterranean fever,[24] in which it reduces attacks and the long-term risk of amyloidosis.[28]

Colchicine is effective for prevention of atrial fibrillation after cardiac surgery.[29] It also decreases the risk of cardiovascular disease in those at high risk; however, has not effect on risk of death in this population.[11]


The typical dose for gout is 0.6 mg once to twice per day.[2] Generally only a few days are taken.[30] Lower doses may be used in those who take certain other medications.[2] The defined daily dose is 1 mg by mouth or by injection.[5]


Long-term treatment with colchicine by mouth are absolutely contraindicated in people with advanced kidney failure (including those on dialysis).[21] About 10-20 percent of a colchicine dose is excreted unchanged by the kidneys; it is not removed by hemodialysis. Cumulative toxicity is a high probability in this clinical setting, and a severe neuromyopathy may result. The presentation includes a progressive onset of proximal weakness, elevated creatine kinase, and sensorimotor polyneuropathy. Colchicine toxicity can be potentiated by the concomitant use of cholesterol-lowering drugs.[21]

Side effects

Deaths – both accidental and intentional – have resulted from overdose of colchicine.[21] Typical side effects of moderate doses may include gastrointestinal upset, diarrhea, and neutropenia.[16] High doses can also damage bone marrow, lead to anemia, and cause hair loss. All of these side effects can result from inhibition of mitosis,[31] which may include neuromuscular toxicity and rhabdomyolysis.[21]


Colchicine poisoning by overdose (range of acute doses of 7 to 26 mg) begins with a gastrointestinal phase occurring 10–24 hours after ingestion, followed by multiple organ dysfunction occurring 24 hours to 7 days after ingestion, after which the affected person either declines into multi-organ failure or recovers over several weeks.[32]

Colchicine can be toxic when ingested, inhaled, or absorbed in the eyes.[16] Colchicine can cause a temporary clouding of the cornea and be absorbed into the body, causing systemic toxicity. Symptoms of colchicine overdose start 2 to 24 hours after the toxic dose has been ingested and include burning in the mouth and throat, fever, vomiting, diarrhea, and abdominal pain.[21] This can cause hypovolemic shock due to extreme vascular damage and fluid loss through the gastrointestinal tract, which can be fatal.[32][33]

If the affected person survives the gastrointestinal phase of toxicity, they may experience multiple organ failure and critical illness. This includes kidney damage, which causes low urine output and bloody urine; low white blood cell counts that can last for several days; anemia; muscular weakness; liver failure; hepatomegaly; bone marrow suppression; thrombocytopenia; and ascending paralysis leading to potentially fatal respiratory failure. Neurologic symptoms are also evident, including seizures, confusion, and delirium; children may experience hallucinations. Recovery may begin within six to eight days and begins with rebound leukocytosis and alopecia as organ functions return to normal.[32][31]

Long-term exposure to colchicine can lead to toxicity, particularly of the bone marrow, kidney, and nerves. Effects of long-term colchicine toxicity include agranulocytosis, thrombocytopenia, low white blood cell counts, aplastic anemia, alopecia, rash, purpura, vesicular dermatitis, kidney damage, anuria, peripheral neuropathy, and myopathy.[31]

No specific antidote for colchicine is known, but supportive care is used in cases of overdose. In the immediate period after an overdose, monitoring for gastrointestinal symptoms, cardiac dysrhythmias, and respiratory depression is appropriate,[31] and may require gastrointestinal decontamination with activated charcoal or gastric lavage.[32][33]

Mechanism of toxicity

With overdoses, colchicine becomes toxic as an extension of its cellular mechanism of action via binding to tubulin.[32] Cells so affected undergo impaired protein assembly with reduced endocytosis, exocytosis, cellular motility, and interrupted function of heart cells, culminating in multi-organ failure.[8][32]


In the United States, there are several hundred recorded cases of colchicine toxicity annually; approximately 10% of which end with serious morbidity or mortality. Many of these cases are intentional overdoses, but others were accidental; for example, if the drug was not dosed appropriately for kidney function. Most cases of colchicine toxicity occur in adults. Many of these adverse events resulted from the use of intravenous colchicine.[27]


Colchicine interacts with the P-glycoprotein transporter, and the CYP3A4 enzyme involved in drug and toxin metabolism.[21][32] Fatal drug interactions have occurred when colchicine was taken with other drugs that inhibit P-glycoprotein and CYP3A4, such as erythromycin or clarithromycin.[21]

People taking macrolide antibiotics, ketoconazole or cyclosporine, or those who have liver or kidney disease, should not take colchicine, as these drugs and conditions may interfere with colchicine metabolism and raise its blood levels, potentially increasing its toxicity abruptly.[21][32] Symptoms of toxicity include gastrointestinal upset, fever, muscle pain, low blood cell counts, and organ failure.[16][21] People with HIV/AIDS taking atazanavir, darunavir, fosamprenavir, indinavir, lopinavir, nelfinavir, ritonavir, or saquinavir may experience colchicine toxicity.[21] Grapefruit juice and statins can also increase colchicine concentrations.[21]

Mechanism of action

In gout, inflammation in joints results from the precipitation of circulating uric acid, exceeding its solubility in blood and depositing as crystals of monosodium urate in and around synovial fluid and soft tissues of joints.[8] These crystal deposits cause inflammatory arthritis, which is initiated and sustained by mechanisms involving various proinflammatory mediators, such as cytokines.[8] Colchicine accumulates in white blood cells and affects them in a variety of ways: decreasing motility, mobilization (especially chemotaxis) and adhesion.[27]

Under preliminary research are various mechanisms by which colchicine may interfere with gout inflammation:

Generally, colchicine appears to inhibit multiple proinflammatory mechanisms, while enabling increased levels of anti-inflammatory mediators.[8] Apart from inhibiting mitosis, colchicine inhibits neutrophil motility and activity, leading to a net anti-inflammatory effect, which has efficacy for inhibiting or preventing gout inflammation.[8][21]


The plant source of colchicine, the autumn crocus (Colchicum autumnale), was described for treatment of rheumatism and swelling in the Ebers Papyrus (circa 1500 BC), an Egyptian medical papyrus.[34] It is a toxic alkaloid and secondary metabolite.[16][35][21] Colchicum extract was first described as a treatment for gout in De Materia Medica by Pedanius Dioscorides, in the first century AD. Use of the bulb-like corms of Colchicum to treat gout probably dates to around 550 AD, as the "hermodactyl" recommended by Alexander of Tralles. Colchicum corms were used by the Persian physician Avicenna, and were recommended by Ambroise Paré in the 16th century, and appeared in the London Pharmacopoeia of 1618.[36][27] Colchicum use waned over time, likely due to the severe gastrointestinal side effects preparations caused. In 1763, Colchicum was recorded as a remedy for dropsy (now called edema) among other illnesses.[27] Colchicum plants were brought to North America by Benjamin Franklin, who had gout himself and had written humorous doggerel about the disease during his stint as United States Ambassador to France.[37]

Colchicine was first isolated in 1820 by the French chemists P. S. Pelletier and J. B.Caventou.[38] In 1833, P. L. Geiger purified an active ingredient, which he named colchicine.[39] It quickly became a popular remedy for gout.[27] The determination of colchicine's structure required decades, although in 1945, Michael Dewar made an important contribution when he suggested that, among the molecule's three rings, two were seven-member rings.[40] Its pain-relieving and anti-inflammatory effects for gout were linked to its ability to bind with tubulin.

United States Unapproved Drugs Initiative

An unintended consequence of the 2006 U.S. Food and Drug Administration (FDA) safety program called the Unapproved Drugs Initiative—through which the FDA sought more rigorous testing of efficacy and safety of colchicine and other unapproved drugs[41]—was a price increase of 2000 percent [42] for "a gout remedy so old that the ancient Greeks knew about its effects."[42] Under Unapproved Drugs Initiative small companies like URL Pharma, a Philadelphia drugmaker, were rewarded with licenses for testing of medicines like colchicine. In 2009, the FDA reviewed a New Drug Application for colchicine submitted by URL Pharma. URL Pharma did the testing, gained FDA formal approval and was granted rights over colchicine. With this monopoly pricing power, the price of colchicine increased.

In 2012 Asia's biggest drugmaker, Takeda Pharmaceutical Co., acquired URL Pharma for $800 million including the rights to colchicine (brand name Colcrys) earning $1.2 billion in revenue by raising the price even more.[42]

Oral colchicine had been used for many years as an unapproved drug with no FDA-approved prescribing information, dosage recommendations, or drug interaction warnings.[43] On July 30, 2009 the FDA approved colchicine as a monotherapy for the treatment of three different indications (familial Mediterranean fever, acute gout flares, and for the prophylaxis of gout flares[43]), and gave URL Pharma a three-year marketing exclusivity agreement[44] in exchange for URL Pharma doing 17 new studies and investing $100 million into the product, of which $45 million went to the FDA for the application fee. URL Pharma raised the price from $0.09 per tablet to $4.85, and the FDA removed the older unapproved colchicine from the market in October 2010, both in oral and intravenous forms, but gave pharmacies the opportunity to buy up the older unapproved colchicine.[45] Colchicine in combination with probenecid has been FDA-approved prior to 1982.[44]

July 29, 2009, colchicine won FDA approval in the United States as a stand-alone drug for the treatment of acute flares of gout and familial Mediterranean fever.[46][47] It had previously been approved as an ingredient in an FDA-approved combination product for gout. The approval was based on a study in which two doses (1.2 mg and 0.6 mg) an hour apart were as effective as higher doses in combating the acute flare of gout.[20]

Marketing exclusivity in the United States

As a drug antedating the FDA, colchicine was sold in the United States for many years without having been reviewed by the FDA for safety and efficacy. The FDA reviewed approved colchicine for gout flares, awarding Colcrys a three-year term of market exclusivity, prohibiting generic sales, and increasing the price of the drug from $0.09 to $4.85 per tablet.[48][49][50]

Numerous consensus guidelines, and previous randomized controlled trials, had concluded that colchicine is effective for acute flares of gouty arthritis. However, as of 2006, the drug was not formally approved by the FDA, owing to the lack of a conclusive randomized control trial (RCT). Through the Unapproved Drugs Initiative, the FDA sought more rigorous testing of efficacy and safety of colchicine and other unapproved drugs.[41] In exchange for paying for the costly testing, the FDA gave URL Pharma three years of market exclusivity for its Colcrys brand,[51] under the Hatch-Waxman Act, based in part on URL-funded research in 2007, including pharmacokinetic studies and a randomized control trial with 185 patients with acute gout.

In April 2010, an editorial in the New England Journal of Medicine said that the rewards of this legislation are not calibrated to the quality or value of the information produced, that no evidence of meaningful improvement to public health was seen, and that it would be less expensive for the FDA, the National Institutes of Health or large insurers to pay for trials themselves. Furthermore, the cost burden of this subsidy falls primarily on patients or their insurers.[52] In September 2010, the FDA ordered a halt to marketing unapproved single-ingredient oral colchicine.[53]

Colchicine patents expire on February 10, 2029.[54]

Orphan drug

URL Pharma also received seven years of market exclusivity for Colcrys in treatment of familial Mediterranean fever, under the Orphan Drug Law. URL Pharma then raised the price per tablet from $0.09 to $4.85 and sued to remove other versions from the market, increasing annual costs for the drug to U.S. state Medicaid programs from $1 million to $50 million. Medicare also paid significantly higher costs, making this a direct money-loser for the government. (In a similar case, thalidomide was approved in 1998 as an orphan drug for leprosy and in 2006 for multiple myeloma.)[52]

Society and culture


It is available as a generic medication in the United Kingdom, where a month's supply costs the NHS about £7.27 as of 2019.[7] In the United States, the wholesale cost of this amount is about US$252.20.[12] In 2017, it was the 201st most commonly prescribed medication in the United States, with more than two million prescriptions.[13][14]


It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities.[55]

Formulations and dosing

Trade names for colchicine are Colcrys or Mitigare which are manufactured as a dark– and light-blue capsule having a dose of 0.6 mg.[21][56] Colchicine is also prepared as a white, yellow, or purple pill (tablet) having a dose of 0.6 mg.[56]

Colchicine is typically prescribed to mitigate or prevent the onset of gout, or its continuing symptoms and pain, using a low-dose prescription of 0.6 to 1.2 mg per day, or a high-dose amount of up to 4.8 mg in the first 6 hours of a gout episode.[4][21][19] With an oral dose of 0.6 mg, peak blood levels occur within one to two hours.[35] For treating gout, the initial effects of colchicine occur in a window of 12 to 24 hours, with a peak within 48 to 72 hours.[21] It has a narrow therapeutic window, requiring monitoring of the subject for potential toxicity.[21] Colchicine is not a general pain relief drug, and is not used to treat pain in other disorders.[21]


According to laboratory research, the biosynthesis of colchicine involves the amino acids phenylalanine and tyrosine as precursors. Giving radioactive phenylalanine-2-14C to C. byzantinum, another plant of the family Colchicaceae, resulted in its incorporation into colchicine.[57] However, the tropolone ring of colchicine resulted from the expansion of the tyrosine ring. Radioactive feeding experiments of C. autumnale revealed that colchicine can be synthesized biosynthetically from (S)-autumnaline. That biosynthesic pathway occurs primarily through a phenolic coupling reaction involving the intermediate isoandrocymbine. The resulting molecule undergoes O-methylation directed by S-adenosylmethionine. Two oxidation steps followed by the cleavage of the cyclopropane ring leads to the formation of the tropolone ring contained by N-formyldemecolcine. N-formyldemecolcine hydrolyzes then to generate the molecule demecolcine, which also goes through an oxidative demethylation that generates deacetylcolchicine. The molecule of colchicine appears finally after addition of acetyl-coenzyme A to deacetylcolchicine.[58][59]



Colchicine may be purified from Colchicum autumnale (autumn crocus) or Gloriosa superba (glory lily). Concentrations of colchicine in C. autumnale peak in the summer, and range from 0.1% in the flower to 0.8% in the bulb and seeds.[27]

Botanical use

Colchicine is widely used in plant breeding by inducing polyploidy in plant cells to produce new or improved varieties, strains and cultivars.[60] Since chromosome segregation is driven by microtubules, colchicine is used in plant cells during cellular division by inhibiting chromosome segregation during meiosis; half the resulting gametes, therefore, contain no chromosomes, while the other half contains double the usual number of chromosomes (i.e., diploid instead of haploid, as gametes usually are), and lead to embryos with double the usual number of chromosomes (i.e., tetraploid instead of diploid).[60] While this would be fatal in most higher animal cells, in plant cells it is not only usually well tolerated, but also frequently results in larger, hardier, faster-growing, and in general more desirable plants than the normally diploid parents. For this reason, this type of genetic manipulation is frequently used in breeding plants commercially.[60]

When such a tetraploid plant is crossed with a diploid plant, the triploid offspring are usually sterile (unable to produce fertile seeds or spores), although many triploids can be propagated vegetatively. Growers of annual triploid plants not readily propagated cannot produce a second-generation crop from the seeds (if any) of the triploid crop, and need to buy triploid seed from a supplier each year. Many sterile triploid plants, including some trees and shrubs, are becoming increasingly valued in horticulture and landscaping because they do not become invasive species. In certain species, colchicine-induced triploidy has been used to create "seedless" fruit, such as seedless watermelons (Citrullus lanatus). Since most triploids do not produce pollen themselves, such plants usually require cross-pollination with a diploid parent to induce fruit production.

The ability of colchicine to induce polyploidy can be also exploited to render infertile hybrids fertile, for example in breeding triticale (× Triticosecale) from wheat (Triticum spp.) and rye (Secale cereale). Wheat is typically tetraploid and rye diploid, with their triploid hybrid infertile; treatment of triploid triticale with colchicine gives fertile hexaploid triticale. When used to induce polyploidy in plants, colchicine cream is usually applied to a growth point of the plant, such as an apical tip, shoot, or sucker. Also, seeds can be presoaked in a colchicine solution before planting.[61]


A clinical trial of 6000 people with COVID-19 infection, funded by the Government of Quebec, began in March 2020 to test the potential efficacy of using colchicine over a 30-day period to reduce disease symptoms.[62]


  1. 1.0 1.1 Shekelle PG, Newberry SJ, FitzGerald JD, Motala A, O'Hanlon CE, Tariq A, et al. (January 2017). "Management of Gout: A Systematic Review in Support of an American College of Physicians Clinical Practice Guideline". Annals of Internal Medicine. 166 (1): 37–51. doi:10.7326/M16-0461. PMID 27802478.
  2. 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 2.8 2.9 "Colchicine Monograph for Professionals". American Society of Health-System Pharmacists. Archived from the original on 27 March 2019. Retrieved 27 March 2019.
  3. 3.0 3.1 Schachner, Lawrence A.; Hansen, Ronald C. (2011). Pediatric Dermatology E-Book. Elsevier Health Sciences. p. 177. ISBN 9780723436652. Archived from the original on 2019-03-27. Retrieved 2019-03-27.
  4. 4.0 4.1 4.2 "Colchicine for acute gout: updated information about dosing and drug interactions". National Prescribing Service, Australia. 14 May 2010. Archived from the original on 30 June 2012. Retrieved 14 May 2010.
  5. 5.0 5.1 "WHOCC - ATC/DDD Index". Archived from the original on 19 August 2020. Retrieved 9 September 2020.
  6. Hutchison, Stuart J. (2009). Pericardial Diseases: Clinical Diagnostic Imaging Atlas with DVD. Elsevier Health Sciences. p. 58. ISBN 9781416052746. Archived from the original on 2019-03-27. Retrieved 2019-03-27.
  7. 7.0 7.1 7.2 7.3 British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. pp. 1085–1086. ISBN 9780857113382.
  8. 8.0 8.1 8.2 8.3 8.4 8.5 8.6 8.7 8.8 8.9 Dalbeth N, Lauterio TJ, Wolfe HR (October 2014). "Mechanism of action of colchicine in the treatment of gout". Clinical Therapeutics. 36 (10): 1465–79. doi:10.1016/j.clinthera.2014.07.017. PMID 25151572. Archived from the original on 2021-08-28. Retrieved 2018-08-19.
  9. Wall, Wilson John (2015). The Search for Human Chromosomes: A History of Discovery. Springer. p. 88. ISBN 9783319263366. Archived from the original on 2019-03-27. Retrieved 2019-03-27.
  10. "Colchicine capsule". DailyMed. Archived from the original on 27 March 2019. Retrieved 27 March 2019.
  11. 11.0 11.1 Ton, Joey (4 October 2021). "#299 Cardiovascular prevention trials: Now calling colchicine to the stand". CFPCLearn. Archived from the original on 25 March 2023. Retrieved 14 June 2023.
  12. 12.0 12.1 "NADAC as of 2019-02-27". Centers for Medicare and Medicaid Services. Archived from the original on 2019-03-06. Retrieved 3 March 2019.
  13. 13.0 13.1 "The Top 300 of 2020". ClinCalc. Archived from the original on 12 February 2021. Retrieved 11 April 2020.
  14. 14.0 14.1 "Colchicine - Drug Usage Statistics". ClinCalc. Archived from the original on 8 July 2020. Retrieved 11 April 2020.
  15. Chen LX, Schumacher HR (October 2008). "Gout: an evidence-based review". Journal of Clinical Rheumatology. 14 (5 Suppl): S55-62. doi:10.1097/RHU.0b013e3181896921. PMID 18830092.
  16. 16.0 16.1 16.2 16.3 16.4 16.5 "Colcrys (colchicine, USP) tablets 0.6 mg. Drug Approval Package". US Food and Drug Administration. 17 February 2010. Archived from the original on 20 June 2019. Retrieved 19 August 2018.
  17. "Information for Healthcare Professionals: New Safety Information for Colchicine (marketed as Colcrys)". U.S. Food and Drug Administration. Archived from the original on 2009-10-18. Retrieved 2019-12-16.
  18. Laubscher T, Dumont Z, Regier L, Jensen B (December 2009). "Taking the stress out of managing gout". Canadian Family Physician. 55 (12): 1209–12. PMC 2793228. PMID 20008601.
  19. 19.0 19.1 19.2 19.3 van Echteld I, Wechalekar MD, Schlesinger N, Buchbinder R, Aletaha D (August 2014). "Colchicine for acute gout". The Cochrane Database of Systematic Reviews. 8 (8): CD006190. doi:10.1002/14651858.CD006190.pub2. PMID 25123076.
  20. 20.0 20.1 Terkeltaub RA, Furst DE, Bennett K, Kook KA, Crockett RS, Davis MW (April 2010). "High versus low dosing of oral colchicine for early acute gout flare: Twenty-four-hour outcome of the first multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose-comparison colchicine study". Arthritis and Rheumatism. 62 (4): 1060–8. doi:10.1002/art.27327. PMID 20131255.
  21. 21.00 21.01 21.02 21.03 21.04 21.05 21.06 21.07 21.08 21.09 21.10 21.11 21.12 21.13 21.14 21.15 21.16 21.17 21.18 21.19 21.20 21.21 "Colchicine". 1 January 2017. Archived from the original on 20 August 2018. Retrieved 19 August 2018.
  22. Shekelle, Paul G.; Newberry, Sydne J.; FitzGerald, John D.; Motala, Aneesa; O'Hanlon, Claire E.; Tariq, Abdul; Okunogbe, Adeyemi; Han, Dan; Shanman, Roberta (2017). "Management of gout: A systematic review in support of an American College of Physicians Clinical Practice Guideline". Annals of Internal Medicine. 166 (1): 37–51. doi:10.7326/M16-0461. ISSN 0003-4819. PMID 27802478.
  23. Qaseem, Amir; Harris, Russell P.; Forciea, Mary Ann (2017). "Management of acute and recurrent gout: A Clinical Practice Guideline From the American College of Physicians". Annals of Internal Medicine. 166 (1): 58–68. doi:10.7326/M16-0570. ISSN 0003-4819. PMID 27802508.
  24. 24.0 24.1 24.2 Cocco G, Chu DC, Pandolfi S (December 2010). "Colchicine in clinical medicine. A guide for internists". European Journal of Internal Medicine. 21 (6): 503–8. doi:10.1016/j.ejim.2010.09.010. PMID 21111934.
  25. Puéchal X, Terrier B, Mouthon L, Costedoat-Chalumeau N, Guillevin L, Le Jeunne C (March 2014). "Relapsing polychondritis". Joint, Bone, Spine. 81 (2): 118–24. doi:10.1016/j.jbspin.2014.01.001. PMID 24556284.
  26. Alabed S, Cabello JB, Irving GJ, Qintar M, Burls A (August 2014). "Colchicine for pericarditis" (PDF). The Cochrane Database of Systematic Reviews. 8 (8): CD010652. doi:10.1002/14651858.CD010652.pub2. PMID 25164988. Archived (PDF) from the original on 2017-09-22. Retrieved 2019-09-24.
  27. 27.0 27.1 27.2 27.3 27.4 27.5 27.6 27.7 27.8 27.9 Goldfrank's toxicologic emergencies. Nelson, Lewis, 1963- (Eleventh ed.). New York. 2019-04-11. ISBN 978-1-259-85961-8. OCLC 1020416505.{{cite book}}: CS1 maint: others (link)
  28. Portincasa P (2016). "Colchicine, Biologic Agents and More for the Treatment of Familial Mediterranean Fever. The Old, the New, and the Rare". Current Medicinal Chemistry. 23 (1): 60–86. doi:10.2174/0929867323666151117121706. PMID 26572612.
  29. Lennerz C, Barman M, Tantawy M, Sopher M, Whittaker P (December 2017). "Colchicine for primary prevention of atrial fibrillation after open-heart surgery: Systematic review and meta-analysis" (PDF). International Journal of Cardiology. 249: 127–137. doi:10.1016/j.ijcard.2017.08.039. PMID 28918897. Archived (PDF) from the original on 2019-04-27. Retrieved 2019-07-09.
  30. "How and when to take colchicine". 7 December 2022. Archived from the original on 6 April 2023. Retrieved 6 April 2023.
  31. 31.0 31.1 31.2 31.3 "CDC - The Emergency Response Safety and Health Database: Biotoxin: Cochicine". Centers for Disease Control and Prevention, US Department of Health and Human Services. Archived from the original on 9 January 2016. Retrieved 31 December 2015.
  32. 32.0 32.1 32.2 32.3 32.4 32.5 32.6 32.7 Finkelstein Y, Aks SE, Hutson JR, Juurlink DN, Nguyen P, Dubnov-Raz G, Pollak U, Koren G, Bentur Y (June 2010). "Colchicine poisoning: the dark side of an ancient drug". Clinical Toxicology. 48 (5): 407–14. doi:10.3109/15563650.2010.495348. PMID 20586571.
  33. 33.0 33.1 Matt Doogue (2014). "Colchicine – extremely toxic in overdose" (PDF). Christchurch and Canterbury District Health Board, New Zealand. Archived (PDF) from the original on 2 March 2018. Retrieved 23 August 2018.
  34. Graham W, Roberts JB (March 1953). "Intravenous colchicine in the management of gouty arthritis" (PDF). Annals of the Rheumatic Diseases. 12 (1): 16–9. doi:10.1136/ard.12.1.16. PMC 1030428. PMID 13031443. Archived (PDF) from the original on 2011-09-29. Retrieved 2010-06-02.
  35. 35.0 35.1 "Colcrys (colchicine). Summary review for regulatory action" (PDF). Center for Drug Evaluation and Research, US Food and Drug Administration. 30 July 2009. Archived (PDF) from the original on 10 February 2017. Retrieved 19 August 2018.
  36. Hartung EF (September 1954). "History of the use of colchicum and related medicaments in gout; with suggestions for further research" (PDF). Annals of the Rheumatic Diseases. 13 (3): 190–200. doi:10.1136/ard.13.3.190. PMC 1006735. PMID 13198053. Archived (PDF) from the original on 2011-09-29. Retrieved 2010-06-02. (free BMJ registration required)
  37. Ebadi, Manuchair S. (2007). Pharmacodynamic basis of herbal medicine. ISBN 978-0-8493-7050-2.
  38. Pelletier and Caventou (1820) "Examen chimique des plusieurs végétaux de la famille des colchicées, et du principe actif qu'ils renferment. [Cévadille (veratrum sabadilla) ; hellébore blanc (veratrum album) ; colchique commun (colchicum autumnale)]" Archived 2016-05-06 at the Wayback Machine (Chemical examination of several plants of the meadow saffron family, and of the active principle that they contain.) Annales de Chimie et de Physique, 14 : 69-81.
  39. Geiger, Ph. L. (1833) "Ueber einige neue giftige organische Alkalien" Archived 2016-05-06 at the Wayback Machine (On some new poisonous organic alkalis) Annalen der Pharmacie, 7 (3) : 269-280; colchicine is discussed on pages 274-276.
  40. Dewar, Michael J.S. (February 3, 1945). "Structure of colchicine". Letters to Editor. Nature. 155 (3927): 141–142. Bibcode:1945Natur.155..141D. doi:10.1038/155141d0. Dewar did not prove the structure of colchicine; he merely suggested that it contained two seven-membered rings. Colchicine's structure was determined by X-ray crystallography in 1952 King, Murray Vernon; de Vries, J. L.; Pepinsky, Ray (July 1952). "An x-ray diffraction determination of the chemical structure of colchicine". Acta Crystallographica. 5 (4): 437–440. doi:10.1107/S0365110X52001313. Its total synthesis was first accomplished in 1959 Eschenmoser, Albert (1959). "Synthese des Colchicins". Angewandte Chemie. 71 (20): 637–640. doi:10.1002/ange.19590712002.
  41. 41.0 41.1 "FDA Unapproved Drugs Initiative". Archived from the original on 2019-04-23. Retrieved 2019-12-16.
  42. 42.0 42.1 42.2 Langreth, Robert; Koons, Cynthia (6 October 2015). "2,000% Drug Price Surge Is a Side Effect of FDA Safety Program". Bloomberg. Archived from the original on 6 December 2017. Retrieved 27 October 2015.
  43. 43.0 43.1 "FDA Approves Colchicine With Drug Interaction and Dose Warnings". July 2009. Archived from the original on 2011-02-03. Retrieved 2010-07-26.
  44. 44.0 44.1 "Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations". Archived from the original on 2018-01-24. Retrieved 2010-07-26.
  45. "Questions and Answers for Patients and Healthcare Providers Regarding Single-ingredient Oral Colchicine Products". Archived from the original on 2017-05-04. Retrieved 2019-12-16.
  46. "FDA Approves Gout Treatment After Long Years of Use". 3 August 2009. Archived from the original on 5 August 2009. Retrieved 3 August 2009.
  47. Cerquaglia C, Diaco M, Nucera G, La Regina M, Montalto M, Manna R (February 2005). "Pharmacological and clinical basis of treatment of Familial Mediterranean Fever (FMF) with colchicine or analogues: an update". Current Drug Targets. Inflammation and Allergy. 4 (1): 117–24. doi:10.2174/1568010053622984. PMID 15720245. Archived from the original on 2008-12-11. Retrieved 2019-07-06.
  48. Karst, Kurt R. (21 October 2009). "California Court Denies Preliminary Injunction in Lanham Act Case Concerning Unapproved Colchicine Drugs". Archived from the original on 23 November 2009. Retrieved 2 June 2010.
  49. Meyer, Harris (29 December 2009). "The High Price of FDA Approval". Kaiser Health News and the Philadelphia Inquirer. Archived from the original on 16 June 2010. Retrieved 2 June 2010.
  50. Colcrys vs. Unapproved Colchicine Archived 2010-07-02 at the Wayback Machine Statement from URL Pharma
  51. "About Colcrys". Colcrys. URL Pharma. Archived from the original on 26 September 2011. Retrieved 11 September 2011.
  52. 52.0 52.1 Kesselheim AS, Solomon DH (June 2010). "Incentives for drug development--the curious case of colchicine". The New England Journal of Medicine. 362 (22): 2045–7. doi:10.1056/NEJMp1003126. PMID 20393164.
  53. "FDA orders halt to marketing of unapproved single-ingredient oral colchicine". 30 September 2010. Archived from the original on 18 January 2017. Retrieved 16 December 2019.
  54. "Generic Colcrys Availability". Archived from the original on 2016-04-21. Retrieved 2018-01-23.
  55. "40 CFR Appendix A to Part 355, The List of Extremely Hazardous Substances and Their Threshold Planning Quantities". LII / Legal Information Institute. Archived from the original on 2017-11-07. Retrieved 2018-03-11.
  56. 56.0 56.1 "Colchicine images". 6 August 2018. Archived from the original on 21 August 2018. Retrieved 21 August 2018.
  57. Leete E (1963). "The biosynthesis of the alkaloids of Colchicum: The incorporation of phenylalaline-2-C14 into colchicine and demecolcine". J. Am. Chem. Soc. 85 (22): 3666–3669. doi:10.1021/ja00905a030.
  58. Dewick PM (2009). Medicinal natural products: A biosynthetic approach. Wiley. pp. 360–362.
  59. Maier UH, Meinhart HZ (1997). "Colchicine is formed by para para phenol-coupling from autumnaline". Tetrahedron Lett. 38 (42): 7357–7360. doi:10.1016/s0040-4039(97)10011-9.{{cite journal}}: CS1 maint: uses authors parameter (link)
  60. 60.0 60.1 60.2 Griffiths AJF, Gelbart WM, Miller JH (1999). Modern Genetic Analysis: Changes in Chromosome Number. W. H. Freeman, New York. Archived from the original on 2019-01-23. Retrieved 2019-07-19.{{cite book}}: CS1 maint: uses authors parameter (link)
  61. Derman H, Emsweller SL. "The use of colchicine in plant breeding". Retrieved 26 April 2016.
  62. "New clinical study: Potential treatment for coronavirus will be tested in Canada as of today". BioSpace. 2020-03-23. Archived from the original on 2020-04-11. Retrieved 2020-04-11.

External links

External sites:

  • "Colchicine : Biotoxin". Emergency Response Safety and Health Database. 8 November 2017. Archived from the original on 9 January 2016. Retrieved 9 September 2017.