Levamisole Hydrochloride For Goats

Back in stock, Prohibit, a levamisole hydrochloride, is a broad spectrum sheep and cattle drench wormer effective against stomach, intestinal, and lung worms. To use, place one packet in one gallon of water. Dosage for sheep is 1 fl. Packet will dose 128 100 lb. I would bet goats won’t drink it if it is mixed by the gallon. I would recommend you have a bottle of Atropine on hand. The dose is 1cc/100lbs IM if you have a goat react, this is the antidote. Levamisole is a cholinesterase inhibitor, and can be toxic even when dosed correctly.

Levamisole, a common cutting agent in cocaine, made the news recently for its apparent skin-destroying properties – but there's a lot more to the substance than that.

A case study from the 'British Medical Journal' of a woman whose skin and flesh is rotting due to the presence of levamisole in the cocaine she had been taking. Photo courtesy BMJ

Corrupted cocaine sold in Britain is making people's skin rot. Or so we were told last week, when a series of reports warned of the 'flesh eating' cocaine causing people to suffer from a rare blood disorder that makes their flesh decompose and their ears go black. The stories came with images from a gruesome case study in the British Medical Journal, of a woman covered in dark blotches and open sores, looking like something out of a medieval physician's casebook.

Newspapers revealed the culprit: levamisole, a cattle de-worming drug found in '80 percent of cocaine' in the UK. The message being: do a bit of a gear and you'll lose all your skin.

Of course, where there are drugs, a scare story is never far behind – and the first myth to blow away here is that levamisole is any great danger to the general cocaine-snorting public. Despite the hype, the chances of cocaine giving you a blood disorder or rotting your skin are incredibly remote. Unless, that is, you're from northern Finland (which I'll get to later).

Levamisole has, over the last decade, become a major cutting agent in the world's cocaine supplies. Depending on where you live, between 40 to 90 percent of cocaine contains the drug. The British government says around 80 percent of seized cocaine shipments in 2014 contained levamisole. In Spain, a 2012 study found the drug in 57 percent of cocaine, and in Denmark in the same year it was in 90 percent of samples. In Holland, the figure is 60 percent, and in the US the DEA puts it at 73 percent.

While the substance might be found frequently, that doesn't mean cocaine is packed with the stuff. Cocaine purity research carried out by Lana Brockbals at drug identification firm TICTAC, seen exclusively by VICE, found that out of 106 samples of cocaine from an unnamed British festival last year, 83 contained traces of the de-wormer. However, the average concentration of levamisole in each wrap was just over five percent, with most samples containing between 1.5 and five percent of levamisole.

Tests on 5,000 street cocaine samples in the Netherlands between 2011 and 2014 found an average concentration of nine percent. In Spain last year, concentration was found to be, on average, 11.9 percent. The DEA says levamisole takes up nine percent of the average American bag of cocaine. An analysis last year of 103 random cocaine samples from around the world, conducted by the Energy Control drug testing service, found that the average concentration was 11 percent.

So does snorting cocaine that contains five, 10 or even 20 percent levamisole warrant the media hype? After all, there are up to an estimated 21 million cocaine users on the planet – you'd expect the hospitals to be rammed with people losing all their skin. But they're not.

I spoke to Dr Lindy-Anne Korswagen, one of the authors of the BMJ study mentioned in all the papers last week, and a doctor at Sint Franciscus Gasthuis Hospital in Rotterdam. 'Given the fact that many people use cocaine, of which large percentages are adulterated with levamisole, our case is rare,' she said. 'The risk of side effects such as agranulocytosis or levamisole-induced vasculopathy with skin ulcers and serious organ damage is small. Between 2011 and 2014, there were 210 cases reported worldwide, of which three have died.'

Dr Korswagen did warn that there may be undiagnosed cases out there.

(Photo by Andoni Lubaki)

The authors of a similar case study (someone suffering from a levamisole-induced skin disease) published in a US medical journal in 2013 said most victims they had come across were heavy cocaine users. 'Many of these affected individuals are chronic, habitual cocaine users, suggesting a large cumulative exposure to cocaine and, by association, levamisole, possibly over an extended period of time.'

Levamisole Injectable Wormer

Toxicologist Dr Robert Hoffman, an expert in levamisole from the New York University Langone Medical Center, told me the amount of the drug found in the average bag of cocaine 'is probably too low' to affect most users, and that when levamisole was used as a legitimate pharmaceutical in medical trials, most patients tolerated full therapeutic doses without a problem. 'Let's say the typical dose of cocaine might be 100mg, so there could be 10mg of levamisole in each dose of cocaine used. Currently, there are still trials where levamisole is used and a dose might be on the order of 150mg over a day. To get that much levamisole, you would have to use a lot of cocaine,' he said. 'So yes, to an extent, the low concentration is somewhat protective in that the total daily dose will be low.'

But it turns out it may not just be about dose; Dr Hoffman told me the evidence points to some people having a genetic vulnerability to the toxic effects of the drug. 'The literature suggests that some patients have a unique genetic predisposition that increases their risk of toxicity,' he said. 'There is always some consideration for dose, but it is a combination of dose plus susceptibility that sets the risk. Luckily for cocaine users, the known responsible genetic abnormality is very uncommon.'

The gene in question, HLA-B27, is present in about eight percent of caucasians, four percent of North Africans, two to nine percent of Chinese and 0.1 to 0.5 percent of Japanese. Oddly, in Lapland in northern Finland, a quarter of people have the gene.

That levamisole is far less of a threat to human health than the media is making out is really no surprise. In such a hugely profitable business as the cocaine trade, you're not going to do all that well making a product that turns your global customer base into a mass of sick or dying invalids – Imperial Tobacco and Philip Morris excluded. Instead, the use of a cattle de-wormer in cocaine is an indicator of how astute the cocaine cartels really are, because they appear to have unearthed the most efficient cocaine-cutting agent of all time.

READ ON MOTHERBOARD: I Went on a 'Make Your Own Cocaine' Tour in Colombia

A report due to be published later this year by a specialist unit dedicated to monitoring the chemicals used to produce cocaine, attached to the UN Office on Drugs and Crime (UNODC), found the use of levamisole to be far from anomalous. It is a strategy based on a firm business and scientific footing.

Conducted by PRELAC (Prevention of the Diversion of Chemical Precursor Substances of Drugs in the Latin America and the Caribbean Countries), the study reveals Colombian firms were the first to start using levamisole a decade ago. Now it's also used by cartels in Peru and Bolivia as the 'cut' of preference for bulking out cocaine before it's exported. In cocaine, levamisole is usually mixed with two other chemicals, such as diltiazem, phenacetin, hydroxyzine and caffeine. For the US and European markets, cocaine is cut 20 percent. If it's going to other countries in South America, such as Brazil, it can be cut to as much as 50 percent.

The authors of the report, 'Dynamics of chemical use in the production of cocaine in the Andean Region', say there are a number of reasons why levamisole has become the number one cut. It's easy to mix with cocaine, has a similar 'fish scale' appearance to high quality cocaine flake and gives the impression of having a greater volume than it actually possesses. It also gives a false positive in street tests for cocaine, so bulk buyers are not able to spot the cocaine has been cut, and is relatively cheap and easily available in bulk from cities across the Andean countries. According to an expert working for the UNODC in Colombia, the drug is regularly purchased at £32 per kilo in Bogota, Cali and Medellin, compared to £1,500 for a kilo of cocaine.

Levamisole Hydrochloride For Goats

According to the UNODC, levamisole is incorporated into cocaine hydrochloride in two stages of the process: before converting cocaine base to cocaine hydrochloride, and later, when the hydrochloride has already been obtained but has not yet dried. So it's in almost everyone's cocaine, even the super rich – although I'd guess there are a few mega-mansions in Colombia and Miami where the cocaine is as pure as it comes.

Levamisole hydrochloride for goats price

WATCH: Cooking Cocaine in Lima

But the game changer – an asset of levamisole of which cartel chemists will be fully aware – is its ability to potentiate the action of cocaine in the body. A metabolite of levamisole called aminorex has amphetamine-like properties, and a growing body of research is beginning to suggest what the Colombian chemists may have known all along: cocaine mixed with levamisole creates an additional high when it's snorted.

'[The cocaine cartels] have extensive financial networks, and we must assume that this drug adds to the potency or addicting qualities of cocaine in a way we have yet to fully determine,' said Dr Hoffman. 'They have access to animal labs and thousands of human subjects, and therefore the addition of levamisole to cocaine is undergoing more testing than most approved drugs.'

These days, cartel chemists are a very different breed to the TV depiction of a guy in a baseball cap stirring a bucket in the middle of the Amazon rainforest. 'It's a mistake to think Colombian cocaine producers are peasants in a jungle lab,' says Mike Power, a journalist and author who has investigated the Colombian cocaine trade. He told me the much-filmed rural farmers (cocaleros) are only part of a big supply line from farmyard to nostril, involving chemistry, airplanes, murder and corruption.

'It would be astonishing if the narco-cartels didn't know about the emerging evidence around the stimulant effects of levamisole,' Power said. 'Four years ago in Colombia, I saw how the crystallisation [of the paste] process was moving from the jungles to underground urban labs, in well guarded apartment blocks. This is a complex science. If they can increase their profits by 10 percent by including an active cut that ticks all the boxes, then it's a no-brainer. And because most of it is being added at end of the process, before export, we know it's being facilitated by people at the high end of the trade. They know exactly what they are doing.'

But, as Power says, the end result for many cocaine users is that while the powder might be white, it's anything but pure. 'The fact is, if you've been using coke,' he said, 'you've been snorting cattle de-wormer for years now, and you're paying through the nose for the privilege.'

@Narcomania

More on VICE:

  • Tagged:
Levamisole
Clinical data
Trade namesErgamisol
AHFS/Drugs.comMicromedex Detailed Consumer Information
MedlinePlusa697011
Routes of
administration
By mouth
ATC code
Legal status
Legal status
  • CA: Withdrawn drug
  • US: Withdrawn
  • Rx-only (RU)
Pharmacokinetic data
MetabolismLiver
Elimination half-life3–4 hours
ExcretionUrine (70%)
Identifiers
  • (S)-6-Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole
CAS Number
  • 14769-73-4
PubChemCID
IUPHAR/BPS
DrugBank
ChemSpider
  • 25037
UNII
KEGG
  • D08114
ChEBI
ChEMBL
  • ChEMBL1454
CompTox Dashboard(EPA)
ECHA InfoCard
Chemical and physical data
FormulaC11H12N2S
Molar mass204.292 g/mol g·mol−1
3D model (JSmol)
Density1.31 g/cm3
Melting point60 °C (140 °F)
  • N2=C1/SCCN1C[C@@H]/2c3ccccc3
  • InChI=1S/C11H12N2S/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10/h1-5,10H,6-8H2/t10-/m1/s1
(what is this?)(verify)

Levamisole, sold under the trade name Ergamisol among others, is a medication used to treat parasitic worm infections.[1] Specifically it is used for ascariasis and hookworm infections.[2] It is taken by mouth.[2]

Levamisole Hydrochloride For Goats Dogs

Side effects may include abdominal pain, vomiting, headache, and dizziness.[2] Use is not recommended during breastfeeding or the third trimester of pregnancy.[2] Serious side effects may include an increased risk of infection.[3] It belongs to the antihelmintic class of medications.[3]

Levamisole was discovered in 1966.[4] It is on the World Health Organization's List of Essential Medicines, the most effective and safe medicines needed in a health system.[5] The wholesale cost in the developing world is about US$0.18 to US$0.33 for a course of treatment.[6] It is not commercially available in the United States.[3] Levamisole is also used as a dewormer for livestock.[7]

  • 1Medical uses

Medical uses[edit]

Worms[edit]

Levamisole was originally used as an anthelmintic to treat worm infestations in both humans and animals. Levamisole works as a nicotinic acetylcholine receptoragonist that causes continued stimulation of the parasitic worm muscles, leading to paralysis. In countries that still permit the use of levamisole, the recommended dose for anthelmintic therapy is a single dose, with a repeated dose 7 days later if needed for a severe hookworm infection.[8] Most current commercial preparations are intended for veterinary use as a dewormer in cattle, pigs, and sheep. However, levamisole has also recently gained prominence among aquarists as an effective treatment for Camallanusroundworm infestations in freshwatertropical fish.[9]

Cancer[edit]

After being pulled from the market in the U.S. and Canada in 1999 and 2003, respectively, levamisole has been tested in combination with fluorouracil to treat colon cancer. Evidence from clinical trials support its addition to fluorouracil therapy to benefit patients with colon cancer. In some of the leukemic cell line studies, both levamisole and tetramisole showed similar effect.[10]

Other[edit]

Levamisole has been used to treat a variety of dermatologic conditions, including skin infections, leprosy, warts, lichen planus, and aphthous ulcers.[11]

An interesting adverse side effect these reviewers reported in passing was 'neurologic excitement'. Later papers, from the Janssen group and others, indicate levamisole and its enantiomer, dexamisole, have some mood-elevating or antidepressant properties, although this was never a marketed use of the drug.[12][13]

Adverse effects[edit]

One of the more serious side effects of levamisole is agranulocytosis, or the depletion of the white blood cells. In particular, neutrophils appear to be affected the most. This occurs in 0.08–5% of the studied populations.[14] There have also been reports of levamisole induced necrosis syndrome in which erythematous painful papules can appear almost anywhere on skin.

It has been used as an adulterant in cocaine resulting in serious side effects.[15][16][17]

Metabolism[edit]

Levamisole is readily absorbed from the gastrointestinal tract and metabolized in the liver. Its time to peak plasma concentration is 1.5–2 hours. The plasma elimination half-life is fairly quick at 3–4 hours which can contribute to not detecting Levamisole intoxication. The metabolite half-life is 16 hours. Levamisole's excretion is primarily through the kidneys, with about 70% being excreted over 3 days. Only about 5% is excreted as unchanged levamisole.[18][19]

Drug testing of racehorse urine has led to the revelation that among levamisole equine metabolites are both pemoline and aminorex, stimulants that are forbidden by racing authorities.[20][21][22] Further testing confirmed aminorex in human and canine urine, meaning that both humans and dogs also metabolize levamisole into aminorex.,[23] though it is unclear whether plasma aminorex is present at any appreciable level. Blood samples following oral administration of levamisole out to 172 hr post-dose did not demonstrate any plasma aminorex levels above that of the limit of quantification (LoQ). Additionally, in cocaine-positive plasma samples, of which 42% contained levamisole, aminorex was never reported at concentrations higher than LoQ.[24]

Detection in body fluids[edit]

Levamisole may be quantified in blood, plasma, or urine as a diagnostic tool in clinical poisoning situations or to aid in the medicolegal investigation of suspicious deaths involving adulterated street drugs. About 3% of an oral dose is eliminated unchanged in the 24-hour urine of humans. A post mortem blood levamisole concentration of 2.2 mg/L was present in a woman who died of a cocaine overdose.[25][26]

Illicit use[edit]

Levamisole has increasingly been used as a cutting agent in cocaine sold around the globe with the highest incidence being in the USA. In 2008–2009, levamisole was found in 69% of cocaine samples seized by the Drug Enforcement Administration (DEA).[15] By April 2011, the DEA reported the adulterant was found in 82% of seizures.[27]

Levamisole adds bulk and weight to powdered cocaine (whereas other adulterants produce smaller 'rocks' of cocaine) and makes the drug appear purer.[28] In a series of investigative articles for The Stranger, Brendan Kiley details other rationales for levamisole's rise as an adulterant: possible stimulant effects, a similar appearance to cocaine, and an ability to pass street purity tests.[29]

Levamisole suppresses the production of white blood cells, resulting in neutropenia and agranulocytosis. With the increasing use of levamisole as an adulterant, a number of these complications have been reported among cocaine users.[15][30][31] Levamisole has also been linked to a risk of vasculitis,[32] and two cases of vasculitic skin necrosis have been reported in users of cocaine adulterated with levamisole.[33]

Levamisole-tainted cocaine was linked to several high-profile deaths. Toxicology reports showed levamisole, along with cocaine, was present in DJ AM's body at the time of his death.[34] Andrew Koppel, son of newsman Ted Koppel, was also found with levamisole in his body after his death was ruled a drug overdose.[35] In 2014 it was suspected to be involved in the death of a Sydney teenager.[36]

In response to the dangers, The Stranger, People's Harm-Reduction Alliance, and DanceSafe began producing tests to identify levamisole's presence in cocaine. The kits include a survey postcard, and one revealed its presence in a 1/4-kg block of cocaine, indicating both users and dealers were using the kits.[37]

Chemistry[edit]

The original synthesis at Janssen Pharmaceutica resulted in the preparation of a racemic mixture of two enantiomers, whose hydrochloride salt was reported to have a melting point of 264–265 °C; the free base of the racemate has a melting point of 87–89 °C. The racemic mixture is referred to as 'tetramisole' - levamisole refers only to the levorotatory enantiomer of tetramisole.

Toxicity[edit]

The LD50 (intravenous, mouse) is 22 mg/kg.[38]

Levamisole Hydrochloride For Goats Sleep

Laboratory use[edit]

Levamisole Hydrochloride For Goats

Levamisole reversibly and noncompetitively inhibits most isoforms of alkaline phosphatase (e.g., human liver, bone, kidney, and spleen) except the intestinal and placental isoform.[39] It is thus used as an inhibitor along with substrate to reduce background alkaline phosphatase activity in biomedical assays involving detection signal amplification by intestinal alkaline phosphatase, for example in in situ hybridization or Western blot protocols.

It is used to immobilize the nematode C. elegans on glass slides for imaging and dissection.[40]

In a C. elegans behavioral assay, analyzing the time course of paralysis provides information about the neuromuscular junction. Levamisole acts as an acetylcholine receptor agonist, which leads to muscle contraction. Continuing activation leads to paralysis. The time course of paralysis provides information about the acetylcholine receptors on the muscle. For example, mutants with fewer acetylcholine receptors may paralyze slower than wild type.[41]

Research[edit]

It has also been studied as a method to stimulate the immune system as part of the treatment of cancer.[42] It has also shown some efficacy in the treatment of nephrotic syndrome in children.[43]

Quicktime player alternative for windows. Method 2: Uninstalling apps From Windows StoreStep 1: Find the QuickTime Player app.

References[edit]

  1. ^Keiser J, Utzinger J (April 2008). 'Efficacy of current drugs against soil-transmitted helminth infections: systematic review and meta-analysis'. JAMA. 299 (16): 1937–48. doi:10.1001/jama.299.16.1937. PMID18430913.
  2. ^ abcdWHO Model Formulary 2008(PDF). World Health Organization. 2009. pp. 86, 590. ISBN9789241547659. Archived(PDF) from the original on 2016-12-13.
  3. ^ abc'Levamisole Advanced Patient Information - Drugs.com'. www.drugs.com. Archived from the original on 20 December 2016. Retrieved 8 December 2016.
  4. ^Prevenier, Martha Howelland Walter (2001). From reliable sources : an introduction to historical methods (1. publ. ed.). Ithaca: Cornell university press. p. 77. ISBN9780801485602. Archived from the original on 2017-09-10.
  5. ^'WHO Model List of Essential Medicines (19th List)'(PDF). World Health Organization. April 2015. Archived(PDF) from the original on 13 December 2016. Retrieved 8 December 2016.
  6. ^'Levamisole'. International Drug Price Indicator Guide. Retrieved 1 December 2016.
  7. ^Taylor, M. A.; Coop, R. L.; Wall, R. L. (2015). Veterinary Parasitology. John Wiley & Sons. p. 329. ISBN9781119073673. Archived from the original on 2017-09-10.
  8. ^'Levamisole (Martindale: The Complete Drug Reference)'. Lexicomp. Archived from the original on 21 December 2016. Retrieved 21 April 2014.
  9. ^Sanford, Shari (2007). 'Levamisole Hydrochloride: Its application and usage in freshwater aquariums'. Loaches Online. Archived from the original on 2009-03-01. Retrieved 2009-02-27.
  10. ^(Chirigos et al. (1969, 1973, 1975)).
  11. ^Scheinfeld N, Rosenberg JD, Weinberg JM (2004). 'Levamisole in dermatology : a review'. American Journal of Clinical Dermatology. 5 (2): 97–104. doi:10.2165/00128071-200405020-00004. PMID15109274.
  12. ^Vanhoutte PM, Van Nueten JM, Verbeuren TJ, Laduron PM (January 1977). 'Differential effects of the isomers of tetramisole on adrenergic neurotransmission in cutaneous veins of dog'. The Journal of Pharmacology and Experimental Therapeutics. 200 (1): 127–40. PMID189006.
  13. ^Przegaliński E, Bigajska K, Siwanowicz J (1980). 'Psychopharmacological profile of dexamisole'. Polish Journal of Pharmacology and Pharmacy. 32 (1): 21–9. PMID7454609.
  14. ^'Levamisole'(PDF). DEA. Archived(PDF) from the original on 17 October 2013. Retrieved 21 April 2014.
  15. ^ abcCenters for Disease Control Prevention (CDC) (December 2009). 'Agranulocytosis associated with cocaine use - four States, March 2008-November 2009'. MMWR. Morbidity and Mortality Weekly Report. 58 (49): 1381–5. PMID20019655.
  16. ^Chang A, Osterloh J, Thomas J (September 2010). 'Levamisole: a dangerous new cocaine adulterant'. Clinical Pharmacology and Therapeutics. 88 (3): 408–11. doi:10.1038/clpt.2010.156. PMID20668440.
  17. ^'Cocaine powder: review of its prevalence, patterns of use and harm'. Advisory Council on the Misuse of Drugs. 12 March 2015.
  18. ^Kouassi E, Caillé G, Léry L, Larivière L, Vézina M (1986). 'Novel assay and pharmacokinetics of levamisole and p-hydroxylevamisole in human plasma and urine'. Biopharmaceutics & Drug Disposition. 7 (1): 71–89. doi:10.1002/bdd.2510070110. PMID3754161.
  19. ^Luyckx M, Rousseau F, Cazin M, Brunet C, Cazin JC, Haguenoer JM, Devulder B, Lesieur I, Lesieur D, Gosselin P, Adenis L, Cappelaere P, Demaille A (1982). 'Pharmacokinetics of levamisole in healthy subjects and cancer patients'. European Journal of Drug Metabolism and Pharmacokinetics. 7 (4): 247–54. doi:10.1007/bf03189626. PMID7166176.
  20. ^Gutierrez, J.; Eisenberg, R.L.; Koval, N.J.; Armstrong, E.R.; Tharappel, J.; Hughes, C.G.; Tobin, T. (August 2010). 'Pemoline and tetramisole 'positives' in English racehorses following levamisole administration'. Irish Veterinary Journal. 63 (8): 498. doi:10.1186/2046-0481-63-8-498. PMC4177197. PMID21777496.
  21. ^Ho EN, Leung DK, Leung GN, Wan TS, Wong AS, Wong CH, Soma LR, Rudy JA, Uboh C, Sams R (April 2009). 'Aminorex and rexamino as metabolites of levamisole in the horse'. Analytica Chimica Acta. 638 (1): 58–68. doi:10.1016/j.aca.2009.02.033. PMID19298880.
  22. ^J. Scarth et al. (2010) 'The use of in vitro drug metabolism studies to complement, reduce and refine in vivo administrations in medication and doping control.' Proceedings of the 18th International Conference of Racing Analyists and Veterinarians. pp 213-222
  23. ^Bertol E, Mari F, Milia MG, Politi L, Furlanetto S, Karch SB (July 2011). 'Determination of aminorex in human urine samples by GC-MS after use of levamisole'. Journal of Pharmaceutical and Biomedical Analysis. 55 (5): 1186–9. doi:10.1016/j.jpba.2011.03.039. PMID21531521.
  24. ^Hess C, Ritke N, Broecker S, Madea B, Musshoff F (May 2013). 'Metabolism of levamisole and kinetics of levamisole and aminorex in urine by means of LC-QTOF-HRMS and LC-QqQ-MS'. Analytical and Bioanalytical Chemistry. 405 (12): 4077–88. doi:10.1007/s00216-013-6829-x. PMID23436169.
  25. ^Vandamme TF, Demoustier M, Rollmann B (1995). 'Quantitation of levamisole in plasma using high performance liquid chromatography'. European Journal of Drug Metabolism and Pharmacokinetics. 20 (2): 145–9. doi:10.1007/bf03226369. PMID8582440.
  26. ^R. Baselt, Disposition of Toxic Drugs and Chemicals in Man, 9th edition, Biomedical Publications, Seal Beach, CA, 2011, pp.901-902. 'Archived copy'(PDF). Archived from the original(PDF) on 2011-09-10. Retrieved 2011-01-22.CS1 maint: archived copy as title (link).
  27. ^Moisse, Katie (2011-06-23). 'Cocaine Laced With Veterinary Drug Levamisole Eats Away at Flesh'. ABC News. Archived from the original on 2011-06-25. Retrieved 2011-06-23.
  28. ^Doheny, Kathleen (Jun 1, 2010). 'Contaminated Cocaine Can Cause Flesh to Rot'. Yahoo!. Archived from the original on 7 June 2010. Retrieved 8 June 2010.
  29. ^Kiley, Brendan (August 17, 2010). 'The Mystery of the Tainted Cocaine'. The Stranger. Archived from the original on December 11, 2010. Retrieved December 21, 2010.
  30. ^Zhu NY, Legatt DF, Turner AR (February 2009). 'Agranulocytosis after consumption of cocaine adulterated with levamisole'. Annals of Internal Medicine. 150 (4): 287–9. doi:10.7326/0003-4819-150-4-200902170-00102. PMID19153405.
  31. ^Kinzie E (April 2009). 'Levamisole found in patients using cocaine'. Annals of Emergency Medicine. 53 (4): 546–7. doi:10.1016/j.annemergmed.2008.10.017. PMID19303517.
  32. ^Menni, Silvano; Pistritto, Grazia; Gianotti, Raffaele; Ghio, Luciana; Edefonti, Alberto (1997). 'Ear Lobe Bilateral Necrosis by Levamisole-Induced Occlusive Vasculitis in a Pediatric Patient'. Pediatric Dermatology. 14 (6): 477–479. doi:10.1111/j.1525-1470.1997.tb00695.x.
  33. ^Bradford M, Rosenberg B, Moreno J, Dumyati G (June 2010). 'Bilateral necrosis of earlobes and cheeks: another complication of cocaine contaminated with levamisole'. Annals of Internal Medicine. 152 (11): 758–9. doi:10.7326/0003-4819-152-11-201006010-00026. PMID20513844.
  34. ^''Kate Plus Eight' is enough'. The San Francisco Chronicle. September 29, 2009. Archived from the original on February 2, 2014. Retrieved January 21, 2014.
  35. ^Parascandola, Rocco (2010-06-18). 'Ted Koppel's son, Andrew Koppel, overdosed on cocktail containing booze, heroin, cocaine and Valium'. Daily News. New York. Archived from the original on 2010-06-22.
  36. ^Olding, Rachel (2014-01-12). 'Young man's death highlights the tragic reality of online illegal drug stores'. Sydney Morning Herald. Sydney. Archived from the original on 2014-01-13.
  37. ^Brendan Kiley (September 11, 2012). 'Now Drug Dealers (Not Just Users) Are Testing Their Cocaine for Levamisole'. The Stranger. Archived from the original on September 28, 2012. Retrieved September 14, 2012.
  38. ^J. Symoens et al. (1979). In Pharmacological and Biochemical Properties of Drug Substances, Vol. 2, (M. E. Goldberg, Ed.), pp. 407-464, Washington: American Pharmaceutical Association.
  39. ^Van Belle H (July 1976). 'Alkaline phosphatase. I. Kinetics and inhibition by levamisole of purified isoenzymes from humans'. Clinical Chemistry. 22 (7): 972–6. PMID6169.
  40. ^'Gonad Dissections Schedl Lab'. Archived from the original on 2014-05-17. Retrieved 2014-05-15. Schedl Lab Protocol for gonad dissections
  41. ^Rand JB (January 2007). 'Acetylcholine'. WormBook: 1–21. doi:10.1895/wormbook.1.131.1. PMC4781110. PMID18050502.
  42. ^Dillman RO (February 2011). 'Cancer immunotherapy'. Cancer Biotherapy & Radiopharmaceuticals. 26 (1): 1–64. doi:10.1089/cbr.2010.0902. PMID21355777.
  43. ^Couderc A, Bérard E, Guigonis V, Vrillon I, Hogan J, Audard V, Baudouin V, Dossier C, Boyer O (December 2017). '[Treatments of steroid-dependent nephrotic syndrome in children]'. Archives de Pediatrie. 24 (12): 1312–1320. doi:10.1016/j.arcped.2017.09.002. PMID29146214.


Retrieved from 'https://en.wikipedia.org/w/index.php?title=Levamisole&oldid=917074089'