Buy Teturam pills 150 mg, 50 pcs
  • Buy Teturam pills 150 mg, 50 pcs


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Clinical Pharmacology

The action of the drug is based on the blockade of acetaldehyde dehydrogenase, which is involved in the metabolism of ethyl alcohol.
This leads to an increase in the metabolite concentration of ethyl alcohol - acetaldehyde, which causes negative sensations (flushing, nausea, vomiting, tachycardia, lowering blood pressure (BP), etc.), which make alcohol use unpleasant after taking Teturam.
This leads to a conditioned reflex aversion to the taste and smell of alcoholic beverages.


Treatment and prevention of recurrence of chronic alcoholism.
As a detoxification agent for chronic nickel poisoning.


1 tablet contains teturam 150 mg

Disulfiram is marketed under different brands and generic names, and comes in different dosage forms:

Brand nameManufacturerCountryDosage form
Teturam Pharmstandard Russia pills
Esperal Sanofi-aventis France pills

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Dosage and Administration

Treatment is prescribed after a thorough examination of the patient and warning about the consequences and complications.
The drug is taken orally on 150-500 mg 2 times a day for an individual scheme.
After 7-10 days, a teturamalcohol sample is taken (20-30 ml of 40% vodka after taking 500 mg of the drug), with a weak reaction, the dose of alcohol is increased by 10-20 ml (the maximum dose of vodka is 100-120 ml).
The sample is repeated after 1-2 days in the hospital and after 3-5 days on an outpatient basis, with the correction of doses of alcohol and / or the drug as needed.
In the future, you can use a maintenance dose of 150-200 mg per day for 1-3 years.

Adverse reactions

"Metallic" taste in the mouth, unpleasant smell (caused by carbon disulphide) in patients with colostomy, hepatitis, lower extremity polyneuropathy, neuropsychiatric disorders, memory loss, disorientation in time and space, asthenia, headache, skin allergic reactions.


Hypersensitivity, thyrotoxicosis, cardiovascular diseases in the stage of decompensation (including pronounced cardiosclerosis, cerebral arteriosclerosis, cerebral vessels pre-and post-infarction, aortic aneurysm, coronary insufficiency, arterial hypertension II-III stage, CHF), heart disease , bronchial asthma, COPD, severe pulmonary emphysema, erosive lesions of the gastrointestinal mucosa, peptic ulcer and 12 duodenal ulcers (in acute stage), bleeding from the gastrointestinal tract, kidney disease, liver failure, sugar di bet, epilepsy, neuro-psychiatric diseases, infectious CNS diseases, polyneuropathy, neuritis of the auditory and optic nerve, glaucoma, cancer, pregnancy, lactation. Age over 60 years, peptic ulcer and 12 duodenal ulcers (in remission), endarteritis, residual cerebrovascular events, psychosis in patients with disulfiram in history.

Drug interactions

Alcohol: intolerance reaction (flushing, erythema, vomiting, tachycardia). Avoid alcohol and drugs containing alcohol.
Unwanted combinations
Isoniazid: impaired behavior and coordination.
Nitro-5-imidazoles (metronidazole, ordinazole, secnidazole, tinidazole): delirious disorders, confusion.
Phenytoin: a significant and rapid rise in the level of phenytoin in plasma with toxic symptoms (suppression of its metabolism).
If combinations cannot be avoided, clinical observation and control of drug concentrations in the plasma of the entry and after treatment with teturam should be carried out.
Combinations that require caution
Warfarin (and other oral anticoagulants): an increased effect of oral anticoagulants and the risk of bleeding (reduction of warfarin in the liver). More frequent monitoring of the concentration of warfarin and adjustment of the dose of anticoagulants within 8 days after discontinuation of teturam is recommended.
Theophylline: teturam inhibits theophylline metabolism. As a result of this, the dose of theophylline should be adjusted (reduced dosage), depending on the clinical symptoms and the plasma concentration of the drug.
Benzodiazepines: teturam can potentiate the sedative effect of benzodiazepines by inhibiting their oxidative metabolism (especially chlordiazepoxide and diazepam). Benzodiazepine dosage should be adjusted according to clinical manifestations.
Tricyclic antidepressants: it is possible to increase the reaction of intolerance to alcohol (especially if patients take teturam on the background, take alcoholic beverages).

Pregnancy and Lactation

Contraindicated during pregnancy and lactation.

Special instructions

Patients should be warned of the dangers of intolerance to alcohol. Teturam should be taken with caution in patients with renal insufficiency or hypothyroidism, especially at risk of a possible combination with alcohol.


Symptoms: the teturam-ethanol combination can cause depression of consciousness up to coma, cardiovascular collapse, neurological complications.
Treatment: symptomatic.

Studies and clinical trials of Disulfiram (Click to expand)
  1. Prenatal exposure to disulfiram implicated in the cause of malformations in discordant monozygotic twins
  2. Determination of Disulfiram by Adsorptive Stripping Voltammetry at Gold Disk Microelectrodes
  3. Reversible, late-onset disulfiram-induced neuropathy and encephalopathy
  4. Arthritis and carpal tunnel syndrome associated with disulfiram (antabuse) therapy
  5. Plasma concentrations of disulfiram after injection of suspended micropellets into alcoholic subjects
  6. Disulfiram is an Inhibitor of Human Purified Monoacylglycerol Lipase, the Enzyme Regulating 2-Arachidonoylglycerol Signaling
  7. Effects of EMD 15,700 and disulfiram on ethanol intake in rats under schedule-induced polydipsia
  8. Disulfiram-mediated inhibition of NF-κB activity enhances cytotoxicity of 5-fluorouracil in human colorectal cancer cell lines
  9. Inhibition of proteasome activity, nuclear factor-KB translocation and cell survival by the antialcoholism drug disulfiram
  10. Antabuse (disulfiram) as a pilot case of nonprofit drug
  11. Antabuse (disulfiram) as an affordable and promising anticancer drug
  12. The effects of disulfiram on the experimental C3H mouse embryo
  13. Peter K. Gessner and Teresa Gessner Disulfiram and its Metabolite Diethyldithiocarbamate. Pharmacology and Status in the Treatment of Alcoholism, HIV Infection, AIDS and Heavy Metal Toxicity Chapman & Hall, London, 1992; 452 pp., £75.00
  14. Effects of disulfiram on serum Dopamine-β-hydroxylase and blood carbon disulphide concentrations in alcoholics
  15. Modulation of synthesis of specific proteins in endothelial cells by copper, cadmium, and disulfiram: An early response to an angiogenic inducer of cell migration
  16. Effects of disulfiram on growth, longevity, and reproduction of the albino rat
  17. Pulse polarographic determination of disulfiram
  18. Colorimetric assay of disulfiram
  19. Reinvestigation of disulfiram-like biological activity of Coprinus atramentarius (Bull. ex Fr.) Fr. Extracts
  20. Sustained-release characteristics of a new implantable formulation of disulfiram
  21. An investigation of Coprinus atramentarius for the presence of disulfiram
  22. Dopamine transporter binding is reduced following disulfiram-induced striatal damage
  23. Imaging evidence of nigral damage in dystonia secondary to disulfiram intoxication
  24. Dystonia and akinesia due to pallidoputaminal lesions after disulfiram intoxication

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