Demeclocycline chemical structure
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Demeclocycline

Demeclocycline (marketed as Declomycin®, Declostatin® and Ledermycin®) is a member of the tetracycline antibiotics group used in various types of bacterial infections. One of its other registered uses is the treatment of hyponatremia (low blood sodium concentration) due to the syndrome of inappropriate antidiuretic hormone (SIADH) where fluid restriction alone has been ineffective. It is derived from the Streptomyces aureofaciens fungal strain. more...

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Mode of action

Its use as an antibiotic is particularly in Lyme disease, acne and bronchitis. Resistance is gradually becoming more common. As with related tetracycline antibiotics, demeclocycline acts by binding to the 30S- and 50S-RNA, which impairs protein synthesis by bacteria. It is therefore bacteriostatic (it impairs bacterial growth but does not kill bacteria directly). Demeclocycline is rarely used for infections.

The use in SIADH actually relies on a side-effect of tetracycline antibiotics; many may cause diabetes insipidus (dehydration due to the inability to concentrate urine). It is not completely understood why demeclocycline impairs the action of antidiuretic hormone, but it is thought that it blocks the binding of the hormone to its receptor.

Side-effects and interactions

These are similar to other tetracyclines. Hypersensitivity may occur. Skin reactions with sunlight have been reported.

Contraindications

As other tetracyclines, demeclocycline is contraindicated in children and pregnant or nursing women. All members of this class interfere with bone development and may discolour teeth.

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Barr Laboratories
From Drug Store News, 1/17/05

Barr Laboratories received approval and began shipment of demeclocycline HCl tablets USP, in 150 mg and 300 mg doses. The drug is the generic equivalent of ESP Pharma's Declomycin, an antibiotic used to treat various types of infections. Barr's demeclocycline HCl will compete in a market with combined annual sales of approximately $40.2 million, based on IMS sales data for the 12 months ended in October.

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COPYRIGHT 2005 Gale Group

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