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Each tablet contains:
The excipients include: povidon, carmelose-sodium,
magnesium stearate and microcrystal cellulose.
Drug Uses :
This medication is used to help treat alcoholism. This drug is not a cure for alcoholism and must be used in combination with supportive
therapy and counseling. This medication must never be used without a person's knowledge.
How to use :
Take this medication by mouth, usually one or two tablets daily as directed by your doctor. Tablets can be crushed or mixed with liquid if
swallowing is a problem. Do not take this medication for at least 12 hours after drinking alcohol.
While taking this medication, it is extremely important you avoid alcohol in all forms including beer, wine, aftershave lotions, mouthwash,
colognes, liquid medications. Read labels carefully, including those of nonprescription products, and ask your pharmacist about the
alcohol content if you are uncertain.
Drug Class and Mechanism :
Disulfiram produces a sensitivity to alcohol which results in a highly unpleasant reaction when the patient under treatment ingests even
small amounts of alcohol. Disulfiram blocks the oxidation of alcohol at the acetaldehyde stage. During alcohol metabolism after
Disulfiram intake, the concentration of acetaldehyde occurring in the blood may be 5 to 10 times higher than that found during metabolism
of the same amount of alcohol alone. Accumulation of acetaldehyde in the blood produces a complex of highly unpleasant symptoms
referred to as the Disulfiram-alcohol reaction. This reaction, which is proportional to the dosage of both Disulfiram and alcohol, will persist
as long as alcohol is being metabolized. Disulfiram does not appear to influence the rate of alcohol elimination from the body.
Missed Dose :
If you miss a dose of Sumycin , take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your
regular dosing schedule. Do not take 2 doses at once.
For Information about Generic Medicines : firstname.lastname@example.org
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range of conditions—from the most common to the most challenging—for people around the world. The Price of the drugs indicated above may
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indicative prices of the drug. The products discussed herein may have different product labelling in different countries. The product information
provided in this site is intended only for the residents of India.
Information for Health Care Professionals
*** Please consult local Prescribing Information for any product before use. This website is an international information resource for healthcare professionals with an interest in disease management. This website is not intended to replace the advice of a qualified healthcare professional. Above brand is a trademark of the Taj group of companies (Taj Pharmaceuticals Limited).
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About Taj Pharmaceutical Limited
Taj Pharmaceuticals Limited
is a pharmaceutical company founded and based in India. The company manufacturers
pharmaceutical formulations and API for India and other countries of world. The company was established in 1995 as an enterprise and
in 2004 became a public limited company. As per Mumbai pharmaxil and Chemixil association the company manufacturers and exports
to countries like Albania, Argentina, Austria, Chile and Iraq. In 1995 pharmaceuticals wing only has a schedule M certification for
pharmaceuticals products manufacturing in India. Taj Pharmaceuticals established its manufacturing unit in Gujarat because of
government policies in 1999 with WHO / GMP licence. The company in 2003 revived all the old manufacturing units and approached the
FDA Gujarat for 4000 new pharmaceuticals drug permissions
for the first time in India.
According to the Indian Trade Mark the company owns about 450 brands and 4600 generic
manufacturing permissions in
India. According to the export data analysis the company was the largest exporter of generic medicines to the Europe and Middle
The company medicines are present in France, Georgia, Egypt and CIF countries.
Taj Pharmaceuticals Limited
Working For Healthier World
Copyright 2011 Taj Pharma Group (India),. All rights reserved.
Copyright 2011 Taj Pharma Group (India),. All rights reserved.
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The Investor Relations section of this website contains forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934. All statements other than statements of historical facts, included on this website regarding the Company's strategy, expected future financial position, results of operations, cash flows, financing plans, discovery and development of products, strategic alliances, competitive position, plans and objectives of management are forward-looking statements. Words such as "anticipate," "believe," "estimate," "expect," "intend," "plan," "will" and other similar expressions help identify forward-looking statements, although not all forward-looking statements contain these identifying words. In particular, any statements regarding the Company's financial results and outlook, the continued implementation of the Company's strategic plan, the development of the Company's pipeline, the commencement of Phase 3 clinical trials for Puricase (pegloticase) are forward-looking statements. These forward-looking statements involve substantial risks and uncertainties and are based on current expectations, assumptions, estimates and projections about the Company's business and the biopharmaceutical and specialty pharmaceutical industries in which the Company operates. Such risks and uncertainties include, but are not limited to, the delay or failure in developing Puricase (pegloticase) and other product candidates; difficulties of expanding the Company's product portfolio through in-licensing or acquisition; not being able to manufacture commercial quantities of our products; not gaining market acceptance sufficient to justify development and commercialization costs if our products are approved for marketing; introduction of generic competition for API; fluctuations in buying patterns of wholesalers; potential future returns of API or other products; the Company continuing to incur substantial net losses for the foreseeable future; difficulties in obtaining financing; potential development of alternative technologies or more effective products by competitors; reliance on third-parties to manufacture, market and distribute many of the Company's products; risks of maintaining protection for the Company's intellectual property; risks of an adverse determination in any future intellectual property litigation; and risks associated with stringent government regulation of the biopharmaceutical and specialty pharmaceutical industries and other factors set forth more fully in certain reports filed with the Securities and Exchange Commission, to which investors are referred for further information. The Company may not actually achieve the plans, intentions or expectations disclosed in its forward-looking statements, and you should not place undue reliance on the Company's forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements that the Company makes. The Company's forward-looking statements do not reflect the potential impact of any future acquisitions, mergers, dispositions, joint ventures or investments that the Company may make. The Company does not have a policy of updating or revising forward-looking statements and assumes no obligation to update any forward-looking statements.
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