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Antabuse

Antabuse can help patients with an alcohol abuse problem not to drink alcohol. When taken with alcohol, this medicine produces unpleasant effects. This medicine is part of a recovery program that includes medical supervision and counseling. It is not a cure.

Other names for this medication:
Chronol, Deadict, Diabuse, Disulfiram, Dulopam, Tyfusin, Ulfiram

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Also known as: Disulfiram

Description

Generic Antabuse is a perfect remedy in struggle against alcoholism. Generic Antabuse acts by blocking the breakdown of alcohol, causing unpleasant side effects (eg, vomiting, upset stomach) when even a small amount of alcohol is consumed. It is an alcohol-abuse deterrent. Antabuse is also known as Disulfiram, Antabus. Generic name of Generic Antabuse is Disulfiram. Brand name of Generic Antabuse is Antabuse.

Dosage

Take Antabuse exactly as directed by your doctor. Follow all directions on your prescription label. Your doctor may occasionally change your dose to make sure you get the best results. Do not take this medicine in larger or smaller amounts or for longer than recommended.

You will need frequent blood tests to check your liver function.

Wear a medical alert tag or carry an ID card stating that you take Antabuse. Any medical care provider who treats you should know that you are using disulfiram.

When Antabuse is used as part of a treatment program for alcohol addiction or detoxification, your doctor may recommend that this medicine be given to you by a family member or other caregiver. This is to make sure you are using the medicine as it was prescribed as part of your treatment.

Additional forms of counseling and/or monitoring may be recommended during treatment.

For best results, keep using this medicine as directed. Antabuse is sometimes given for up to several months or years.

Store at room temperature away from moisture, heat, and light.

Detailed Antabuse dosage information

Overdose

If you overdose Generic Antabuse and you don't feel good you should visit your doctor or health care provider immediately.

Storage

Store at room temperature between 20 and 25 degrees C (68 and 77 degrees F) away from moisture and heat. Keep in a tight light resistant container. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Antabuse are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Do not take Antabuse if you have consumed alcohol within the past 12 hours. Do not drink alcohol while taking disulfiram and for up to 14 days after you stop taking this medicine.

You should not use Antabuse if you are allergic to disulfiram, or if:

you have recently taken metronidazole (Flagyl) or paraldehyde; you have consumed any foods or products that contain alcohol (mouthwash, cough medicine, cooking wine or vinegar, certain desserts, and others). you have severe heart disease or blockage in the arteries of your heart; or you have been diagnosed with psychosis.

To make sure Antabuse is safe for you, tell your doctor if you have:

liver or kidney disease; heart disease, high blood pressure, history of heart attack or stroke; underactive thyroid; diabetes; seizures or epilepsy; head injury or brain damage; mental illness; an allergy to rubber; or if you take phenytoin (Dilantin), tuberculosis medicine, or a blood thinner (warfarin, Coumadin, Jantoven).

It is not known whether Antabuse will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medicine.

It is not known whether Antabuse passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Do not give this medicine to anyone under 18 years old without medical advice.

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The X factor: an Indian perspective on women in academic oncology. The presence of a congenital malformation at birth is a cause of anxiety at an otherwise joyous occasion. Importantly, the fusion of GFP to MKP-3 did not alter the specificity of the phosphatase towards its MAPK substrates. This study suggests the use of SDA as a dietary treatment for obesity. Clinical information was prospectively collected and retrospectively reviewed. In silico analysis of amino acid variation in human respiratory syncytial virus: insights into immunodiagnostics. Comparison of the virulence of wild-type and mutant strains by use of a mouse model system showed that NmlR(sp) and AdhC do not play a key role in the adherence of pneumococci to the nasopharynx in vivo. Thus, whether the decision-making process for therapeutic management of lung cancer patients might be independently affected by COPD remains elusive. Through reverse transcriptase analysis, it was demonstrated that the genes contained in the putative mrk operon were linked and likely to be expressed as a single operon. Genetic differences among populations in sexual dimorphism: evidence for selection on males in a dioecious plant.

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After myocardial infarction, patients with conditions that are often considered contraindications to beta-blockade (such as heart failure, pulmonary disease, and older age) and those with nontransmural infarction benefit from beta-blocker therapy. The observed positive changes in IPSS, PV, and Qmax in men with BPH and the improvement in NIH-CPSI-QoL in patients with CP after using a physiotherapeutic device for six months as mono-therapy, support the view that thermobalancing therapy with the device can be recommended for these patients. The premise of this approach is that disruption of myostatin expression is known to induce muscle hypertrophy and so for Duchenne muscular dystrophy (DMD) could be expected to have a better outcome than dystrophin restoration alone. Limb salvage in malignant tumours of the upper limb using vascularised fibula. We cultured alpha1ABKO myocytes and reconstituted alpha1-AR signaling with adenoviruses expressing alpha1-GFP fusion proteins. Retention period differentially attenuates win-shift/lose-stay relative to win-stay/lose-shift performance in the rat.

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