ABSTRACT
Levamisole is a drug originally prescribed as an antihelmintic. Because of the occurrence of severe cases of agranulocytosis and leukoencephalitis it was removed from the French market in 1998 for human use, while it remains available for veterinary use. Nowadays in France its only use in humans is regulated by authorization for temporary use for its immunomodulatory properties in the treatment of nephritic syndrome.A 52-year-old man was found dead at his farm. Injection points were observed on his arm and a syringe containing a dark orange-brown liquid was found near the body. At his home, the discovery of a letter highlighted suicidal intent. Analysis of the aforementioned liquid, peripheral blood and urine confirmed the unique presence of levamisole. The femoral blood concentration of levamisole was of 25 mg/L whereas the femoral blood concentrations reported in cases of fatalities after cocaine use do not exceed 0.0056 mg/L. In humans, levamisole can be detected in biological samples after cocaine use as this drug is also an adulterant and one of its metabolites (aminorex) seems to have amphetamine-like properties. In this case, the man consumed levamisole from time to time for its stimulant and strengthening effects.Cases of fatal poisoning using levamisole are very rare and poorly documented, which makes the interpretation of postmortem blood levamisole concentration difficult.
Subject(s)
Antinematodal Agents/poisoning , Levamisole/poisoning , Suicide, Completed , Antinematodal Agents/administration & dosage , Antinematodal Agents/analysis , Humans , Injections, Intravenous , Levamisole/administration & dosage , Levamisole/analysis , Male , Middle AgedABSTRACT
Adulteration of cocaine with levamisole is common and can induce serious medical complications. Levamisole is an antihelminthic agent originally approved as an immunomodulator in the treatment of autoimmune disorders and as a chemotherapy adjunct. It was withdrawn from the US market in 2000 but is available in veterinary medicine. Cocaine-using patients may present with nonspecific constitutional symptoms, cutaneous eruptions, leukopenia, vasculitis, and organ damage. Skin manifestations may include severe necrosis, especially of the ear lobes. Here, a case of levamisole toxicity is presented and treatment options are discussed.
Subject(s)
Antinematodal Agents/poisoning , Cocaine-Related Disorders/complications , Cocaine-Related Disorders/diagnosis , Drug Contamination , Levamisole/poisoning , Adult , Female , Humans , Myalgia/chemically induced , Myalgia/diagnosisABSTRACT
A growing number of case reports cite serious health complications linked to the cocaine adulterant, levamisole and women are disproportionately affected; however, the clinical effects are not well established. Between April and October of 2010, we conducted a cross-sectional study among 222 homeless and unstably housed women (116 human immunodeficiency virus [HIV]-infected and 106 HIV-uninfected). Immune markers and behavioral factors were compared in separate models by cocaine and levamisole exposure. Overall, 63% of participants were toxicology positive for cocaine/benzoylecgonine, 85% of whom also tested positive for levamisole. Differences in immune markers did not reach levels of significance among HIV-uninfected persons. Compared to HIV-infected persons who were negative for both cocaine and levamisole, the adjusted odds of low white blood cell count were significantly higher among HIV-infected persons positive for both (p = 0.03), but not for those positive for cocaine only. Neutrophil count and HIV viral load did not differ by cocaine and levamisole status among HIV-infected persons. In a separate model, the adjusted odds of testing positive for levamisole were higher among African American women compared to Caucasian and Asian women (p = 0.02). In the context of high levamisole prevalence, results suggest that decreased immune function as a result of levamisole exposure occurs mainly in individuals who are already immune compromised (e.g., HIV-positive), and race/ethnicity appears to be an important factor in understanding levamisole exposure among cocaine-using women. While larger and geographically diverse studies are needed to elucidate these initial findings, results suggest that levamisole may be one mechanism of immune dysfunction in HIV-infected cocaine-using women.
Subject(s)
Cocaine-Related Disorders/epidemiology , Cocaine/poisoning , HIV Infections/complications , Ill-Housed Persons/statistics & numerical data , Levamisole/poisoning , Adult , Antinematodal Agents/poisoning , Biomarkers/analysis , California/epidemiology , Cross-Sectional Studies , Drug Contamination , Female , HIV Infections/epidemiology , Humans , Logistic Models , Middle Aged , Multivariate Analysis , Self ReportABSTRACT
Levamisole is an immunomodulatory agent that was used to treat various cancers before being withdrawn from the United States market in 2000 because of adverse effects. Levamisole is currently approved as an antihelminthic agent in veterinary medicine, but is also being used illicitly as a cocaine adulterant. Potential complications associated with use of levamisole-laced cocaine include neutropenia, agranulocytosis, arthralgias, retiform purpura, and skin necrosis. Treatment is primarily supportive, and skin lesions typically resolve with cessation of cocaine use. The incidence of hospitalizations related to use of levamisole-contaminated cocaine continues to increase and clinicians should be aware of the more common clinical manifestations.
Subject(s)
Agranulocytosis/chemically induced , Antinematodal Agents/adverse effects , Cocaine/poisoning , Drug Contamination , Levamisole/adverse effects , Purpura/chemically induced , Antinematodal Agents/administration & dosage , Antinematodal Agents/poisoning , Arthralgia/chemically induced , Humans , Levamisole/administration & dosage , Levamisole/poisoning , Retrospective Studies , Vasculitis/chemically inducedABSTRACT
Selected oil cakes, neem, castor and mahua, were tried independently and in combination with a chemical nematicide (carbofuran 3G) for the management of Pratylenchus delattrei in crossandra under glass house conditions. The neem oil cake was effective compared to other oil cakes used and there was a synergistic effect when the neemcake was coupled with carbofuran 3G in the management of Pratylenchus delattrei. The treatment resulted in better establishment of seedlings, and with increased plant bio-mass and flower yield.
Subject(s)
Acanthaceae/parasitology , Antinematodal Agents/poisoning , Carbofuran/poisoning , Castor Oil/poisoning , Fatty Acids/poisoning , Glycerides/poisoning , Terpenes/poisoning , Tylenchoidea/drug effects , Acanthaceae/growth & development , Animals , India , Plant Roots/growth & development , Plant Roots/parasitologyABSTRACT
This study was designed to evaluate possible organ and system disorders associated with experimentally induced levamisole poisoning in dogs. For this purpose, twelve clinically healthy dogs of different ages, sexes and breeds were used. They were divided into two equal groups (Group A and Group B) and given levamisole orally at a dose of 25 mg/kg of body weight daily for three days. The dogs in Group B were also injected with atropin sulphate (0.04 mg/kg of body weight) subcutaneously (sc) 1 hour after each administration of levamisole. Routine clinical examinations were made and some haematological, biochemical and blood gas parameters were established at various times after administration of levamisole. The dogs in Group A developed severe neurological signs, gastric haemorrhage, bloody vomiting, colic, anaemia and four dogs died. In Group B these signs were mild and only one dog died. Levamisole poisoning was characterised by a significant reduction in the total number of red blood cells (RBCs), concentration of haemoglobin (Hb) and packed cell volume (PCV), and by anaemia. Peripheral blood pH, actual bicarbonate of plasma (HCO3), actual base excess (BE), partial pressure of oxygen (pO2) and saturated oxygen (O2SAT) increased in both groups of animals and these dogs developed metabolic alkalosis 48 hours after the first administration of levamisole. The results of the study also show that levamisole poisoning in dogs causes a significant increase in the activity of serum alanine aminotransferase (ALT) and of alkaline phosphatase (AP) and in the concentration of urea in both Group A and Group B. In the study, atropin sulphate reduced the severity of the clinical signs and the number of deaths, but it was not alone sufficient to remedy levamisole poisoning in dogs.
Subject(s)
Antinematodal Agents/poisoning , Dog Diseases/blood , Levamisole/poisoning , Animals , Antinematodal Agents/therapeutic use , Atropine/administration & dosage , Blood Chemical Analysis/veterinary , Blood Gas Analysis/veterinary , Dog Diseases/chemically induced , Dog Diseases/drug therapy , Dogs , Erythrocyte Count/veterinary , Female , Hematocrit/veterinary , Hematologic Tests/veterinary , Hemoglobins/analysis , Levamisole/therapeutic use , Male , Random AllocationABSTRACT
Moxidectin is a macrolide endectocide available as a 2% equine oral gel in the US. This report presents clinical signs of moxidectin toxicosis and its treatment in equines as reported to the ASPCA Animal Poison Control Center (APCC) from January 1998 to December 2000. Nine cases of moxidectin overdose in equines occurred: 5 had signs of toxicosis such as coma, dyspnea, depression, ataxia, tremors, seizures, or weakness. The approximate dose of moxidectin at which these signs were observed ranged from 1.0 to 5.1 mg/kg. The 4 equines that ingested moxidectin between 0.9 mg/kg to 1.7 mg/kg did not show signs of toxicosis. Clinical signs were seen within 6-22 h and lasted for 36-168 h. Only 1/5 clinical equines was an adult, the others were < 4 month of age. This study supports earlier report that young foals are more susceptible to moxidectin toxicosis. All 4 equines with known outcomes recovered with treatment that included decontamination, seizure control, thermoregulation, fluid therapy, and supportive care.
Subject(s)
Anti-Bacterial Agents/poisoning , Antinematodal Agents/poisoning , Horse Diseases/chemically induced , Animals , Animals, Newborn , Anti-Bacterial Agents/administration & dosage , Antinematodal Agents/administration & dosage , Coma/chemically induced , Coma/veterinary , Drug Overdose/veterinary , Dyspnea/chemically induced , Dyspnea/veterinary , Female , Horses , Macrolides , Male , Retrospective Studies , Risk Factors , Seizures/chemically induced , Seizures/veterinaryABSTRACT
A collie, known for its breed-dependent adverse reaction to ivermectin, was without any clinical signs. The dog was prophylactically treated with 3 mg/kg KG (s.c.) of levamisole. Within 15 minutes, the dog showed convulsions, vomitus, and dyspnea, and perished 2.5 hours after injection of the drugs. The pathological findings were not informative as to the cause of death, and with regard to the adverse reactions, additional application of ivermectin was not excluded. Therefore, organ samples were submitted for toxicological analysis of both levamisole and ivermectin. For detection of levamisole and ivermectin, modified GC/MS and HPLC procedures were developed. Concentrations up to 535 micrograms levamisole and up to 26 ng ivermectin were found per g tissue. Both analytical methods are sensitive enough to detect these drugs after application of low doses. This study elucidates that combination of low-dosed ivermectin and levamisole is no recommendable means against adverse effects of ivermectin, with respect to collies. Moreover, the synergistic effects of ivermectin and levamisole suggests the same drug incompatibility in other dog breeds and animal species.
Subject(s)
Antinematodal Agents/analysis , Dog Diseases/chemically induced , Drug Hypersensitivity/veterinary , Ivermectin/analysis , Levamisole/analysis , Adipose Tissue/chemistry , Animals , Antinematodal Agents/administration & dosage , Antinematodal Agents/poisoning , Chromatography, High Pressure Liquid/methods , Chromatography, High Pressure Liquid/veterinary , Dogs , Drug Hypersensitivity/diagnosis , Drug Synergism , Fatal Outcome , Female , Gas Chromatography-Mass Spectrometry/methods , Gas Chromatography-Mass Spectrometry/veterinary , Ivermectin/administration & dosage , Ivermectin/poisoning , Levamisole/administration & dosage , Levamisole/poisoning , Liver/chemistry , Muscles/chemistry , Sensitivity and SpecificityABSTRACT
The poisoning of Costa Rican banana workers by multinational corporations' excessive use of pesticides is not a local issue; it is embedded in a dominant ideology expressed by the phenomenon of globalization. This ideology seeps into every aspect of our social institutions--economic, political, and legal. The practice of this ideological perspective is evident in the industrialization of global agriculture and the shift from "developmentalism"--liberal welfarism, industrialization, and urbanization--to a dominant, undemocratic, global financial elite with "economism" and a neoliberal political agenda overriding the nation-state polis. A specific effect is to transform the agricultural workers of developing countries, such as Costa Rican banana workers, into politically superfluous flesh-and-blood human beings.
Subject(s)
Agriculture/economics , Food Industry/economics , Hazardous Substances/poisoning , Occupational Exposure , Pesticides/poisoning , Propane/analogs & derivatives , Antinematodal Agents/poisoning , Commerce/economics , Commerce/standards , Costa Rica/epidemiology , Food Industry/legislation & jurisprudence , Food Industry/standards , Fruit/parasitology , Humans , Infertility/etiology , International Agencies , Investments , Occupational Exposure/legislation & jurisprudence , Political Systems , Propane/poisoning , Public Policy , Social ResponsibilitySubject(s)
Agricultural Workers' Diseases/diagnosis , Antinematodal Agents/poisoning , Carbamates , Environmental Monitoring/methods , Insecticides/poisoning , Agricultural Workers' Diseases/therapy , Animals , Antinematodal Agents/classification , Antinematodal Agents/pharmacokinetics , Cholinesterases/blood , Cholinesterases/metabolism , First Aid , Humans , Insecticides/classification , Insecticides/pharmacokinetics , Physical Examination , Skin AbsorptionABSTRACT
Pesticides have been used for many years. In earlier times they were a protection against fungi and insect pests. The great increase in the use of pesticides occurred with the development of new organic chemicals following World Wars I and II. In addition to chemicals for the control of fungi and insects, new developments were nematocides, herbicides, rodenticides, avicides, defoliants, wood preservatives, etc. The use of chemicals helped increase productivity, but caused great concern about their effect on human health and safety. On the other hand, chemicals did help tremendously from the standpoint of protecting against diseases that were carried by insects, especially mosquitoes. Adverse publicity has caused great concern about pesticides and this is especially so since our society has undergone great changes from an agricultural society to an industrial society and finally to a communications society. Unfortunately, publicity relating to the use of pesticides has seldom been balanced from the standpoint of the good and the bad. In fact, the communications media has and does usually stress the potential adverse effects of pesticides without reference to the good. This has caused concern on the part of advocates and the average person to the extent that it has placed heavy constraints on agriculture. There is a need for the dissemination of balanced information on the good as well as the bad of pesticides.
Subject(s)
Pesticides/pharmacology , Agricultural Workers' Diseases/chemically induced , Agriculture , Animals , Antinematodal Agents/poisoning , Egg Shell , Environmental Pollutants , Fishes/physiology , Food Contamination , Humans , Legislation, Drug/trends , Oryza , Pesticides/poisoning , Polychlorinated Biphenyls/toxicity , Species Specificity , United States , VegetablesABSTRACT
The agriculturally important nematocide 1,2-dibromo-3-chloropropane (DBCP) has been implicated as a cause of human male sterility. A survey at the Michigan Division of The Dow Chemical Company included measurements of semen samples, testicular size, and serum follicle-stimulating hormone (FSH), luteinizing hormone (LH), and testosterone in 232 chemical workers with past potential exposures to DBCP and in 97 nonexposed comparison employees. Potentially exposed groups showed significantly higher, although not abnormal, mean levels of FSH and LH. In the subgroup with the highest potential exposure ending subsequent to 1972, greater duration of exposure correlated with lower sperm count, higher FSH level, and smaller testicular volume. Mean values for this latter time-divided subgroup were not abnormal. The findings are consistent with a testicular effect of DBCP and also with reversibility of that effect over time.