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DETAILED EXPLANATION OF THE INVENTION
This invention relates to an anti-inflammatory analgesic patch. More specifically the invention relates to an anti-inflammatory analgesic patch containing 4-bi-phenylylacetic acid as the effective ingredient and crotamiton as an absorption
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FIELD OF THE INVENTION
This invention relates to a composition and method for treating patients with mucosal inflammatory disorders, and especially vulvar vestibulitis. Specifically, this invention relates to the topical treatment of erythema and pain of the vulvar vestibule using a nonsteroidal
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BACKGROUND
Macrocyclic lactones, and in particular, the "macrolides" are naturally derived and semi-synthetic compounds that are anti-bacterial, anti-inflammatory and also potentially able to modify ion transport (Saint-Criq et al. 2011 B). These biological activities have resulted in the use of
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FIELD OF THE INVENTION
The present invention concerns a disinfectant or antimicrobial composition that is suitable for use in dental treatment. More in particular, the present invention concerns compositions for use in treating or preventing apical, lateral or marginal periodontitis, gingivitis,
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This application is a request for U.S. examination filed under 35 U.S.C. .sctn.371 of International application No. PCT/JP93/00852 filed on Jun. 21, 1993.
TECHNICAL FIELD
The present invention relates to a novel zinc tranexamate compound and its pharmacologically acceptable organic acid salts, to a
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The present invention relates to a new class of 2-bromo-6-fluoro pregnanes.
More particularly, the present invention relates to 2-bromo-6.beta.-fluoro-3-keto-.DELTA..sup.1,4 -steroids of the pregnane series which possess valuable pharmacological properties, particularly anti-inflammatory and
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BACKGROUND OF THE INVENTION
The present invention relates to novel and useful derivatives of biologically active agents containing a carboxylic acid function.
A wide variety of compounds containing carboxylic acid functions are biologically active. Examples include the non-steroidal
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BACKGROUND OF THE INVENTION
Stratum corneum, the outer layer of skin, is a multicellular membrane of flattened, metabolically active cells. In living animals, the membrane is dynamic, in that surface cells are lost through desquamation but replaced at an equivalent rate from the underlying epidermal
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EXAMPLE I
THERMAL CHALLENGE ANTI-HEMORRHOIDAL ACTIVITY STUDY
The ability of the compounds of formulas (I), (II) and (III) to effectively reduce swelling is demonstrated by the following test:
The right ear of a rat is placed between two metal cylinders held together by a fource of 2 lbs. The
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BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a powdery pharmaceutical composition suitable for application to the mucosa of the oral or nasal cavity. More specifically, it relates to a powdery pharmaceutical composition, suitable for application to the
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CROSS REFERENCE TO RELATED APPLICATIONS
This application is a filing under 35 U.S.C. 371 of International Application No. PCT/GB2016/053695 filed Nov. 24, 2016, entitled "Salts of Tetracyclines" which claims priority to Portuguese Patent Application No. 108978 filed Nov. 24, 2015, which applications
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BACKGROUND
Field of the Disclosure
The present disclosure relates generally to pharmaceutical compositions, and more particularly, to pharmaceutical compositions natural components for treating ear diseases.
Background Information
An example of an ear disease is cauliflower ear, which is a deformity
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The present invention relates to the novel method of treating inflammation in mammals by administering bis-(2-pyridyl-1-oxide) disulfide, the metal salts of bis-(2-pyridyl-1-oxide) disulfide and to novel compositions containing such compounds.
Bis-(2-pyridyl-1-oxide) disulfide (also referred to as
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BACKGROUND OF THE INVENTION
The present invention relates to the novel method of treating inflammation in mammals by administering the synergistic combination of a corticosteroid and at least one metal salt of bis-(2-pyridyl-1-oxide) disulfide and to novel compositions containing such
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FIELD OF THE INVENTION
The present invention relates to novel 6-alkylamino-2,2'-disubstituted-7,8-disubstituted-2H-1-benzopyran derivatives, a method for the preparation thereof using a parallel synthetic method which is one of combinatorial chemical synthetic methods, a use of the novel compounds
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