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Antabuse

Antabuse is a prescription medicine used to treat the symptoms of Alcoholism. Antabuse may be used alone or with other medications. Antabuse belongs to a class of drugs called Psychiatry Agents, Other.

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

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Also known as: Disulfiram

Description

Antabuse (disulfiram) blocks an enzyme that is involved in processing alcohol. Disulfiram produces very unpleasant side effects (such as fast heartbeat, chest pain, nausea, dizziness, flushing, and thirst) when combined with alcohol in the body.

Antabuse is used in certain people with chronic alcoholism. This medicine can help keep you from drinking because of the unpleasant side effects that will occur if you consume alcohol while taking Antabuse.

Antabuse is used together with therapy and counseling support to help you stop drinking. This medicine is not a cure for alcoholism.

Dosage

Do not take the first dose of Generic Antabuse for at least 12 hours after drinking alcohol. Take Generic Antabuse orally with or without food. If you want to achieve most effective results do not stop taking Generic Antabuse suddenly.

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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Our aim was to investigate whether incidental renal artery stenosis (RAS) increases the risk for adverse cardiovascular and renal outcomes in these patients. The main structural element of biological membranes is a liquid-crystalline lipid bilayer. The deduced amino acid sequences of the RLN3-like cDNAs contained the two-chain structure common to relaxin including a RXXXRXXI/V motif in the B-chain. Bioinformatic analysis of xenobiotic reactive metabolite target proteins and their interacting partners. Broadband emission from Cr-doped fibers fabricated by drawing tower. Fifty-one male and female inpatient alcoholics received cue exposure treatment involving in vivo exposure to alcohol cues and imaginal exposure to individualized high-risk drinking situations involving negative emotional cues. Cylindrical nanoholes under 16 nm diameters were well-formed on SiO2 layer. Proximal subungual onychomycosis probably starts with a fungal skin infection, whereas white superficial onychomycosis seems to be a culture of T. Ipsilateral pulmonary vein isolation followed by, if necessary, electrical cardioversion were performed in all patients.

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Intravenous insulin improves clinical outcome in patients hospitalized in intensive care units. Clinical profile of HIV/AIDS-infected patients admitted to a new specialist unit in Dhaka, Bangladesh--a low-prevalence country for HIV. In the present study, we determined the expression and subcellular localization of centrobin in selected mouse tissues. Hyperlipidemia modulates the expression of multiple genes, however, and the effects of PAI-1 on the arterial response to injury under hyperlipidemic conditions are unknown. Insight into molecular and functional diversity of tachykinins and their receptors. Aberrant respiratory sensitivity to CO(2) as a trait of familial panic disorder. Enhancement of MSH receptor- and GAL4-mediated gene transfer by switching the nuclear import pathway. However, the baseline urinary excretion of 8-OHdG before exercise tended to be lower after beta-carotene supplementation.

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CTA is currently widely considered the standard, due to its high accuracy and reliability. To examine the proximal signaling processes mediated by the pre-TCR complex and the role of the TCR-zeta chain in these processes, we stimulated pre-TCR-expressing cells and analyzed the interactions of the TCR/CD3 invariant chains with the Syk/ZAP-70 family of protein tyrosine kinases. We conducted a community-based cross-sectional study including 1083 healthy subjects (323 men and 760 women) in an urban biaxin oral suspension area. Herein we report a several-fold increase in the efficacy of such CPPs if the linear flexible spacer (-X-) in the (R-X-R) motif is replaced by constrained cyclic 1,4-substituted-cyclohexane-derived spacers. Here we report a molecular study of the JT involving 1q21 found in a patient with acute myelomonocytic leukemia that had transformed from myelodysplastic syndrome (MDS). Here we report two cases that illustrate the difficulty in distinguishing between primary and secondary cutaneous involvement. Recognition of the toxin by the anti-alpha-bungarotoxin single chain Fv was very similar to that of the receptor, such as indicated by the epitope mapping of alpha-bungarotoxin through overlapping synthetic peptides.

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