摘要:
The present invention relates to compounds of the general formula (I) and salts and physiologically functional derivatives thereof, for use in the treatment of medical conditions which are caused by an adeno virus, HHV (human herpesvirus), VZV (varicella zoster virus), HSV (herpes simplex virus), EBV (Epstein-Barr virus), vaccinia virus, or BK virus.
摘要:
A silicone gel ("silogel") composition used to deliver pharmaceutical products transdermally as well as a method for producing the silogel composition, which may contain up to 80% additive ingredients. Preferred embodiments of the invention may include silogel compositions which provide high viscosity/no separation due to API. They are not temperature- sensitive, have no shear stress from the ointment mill/EMP, have no gumming up/stickiness, and no hardening.
摘要:
The present invention provides a stable, aqueous solution comprising bromfenac or a pharmacologically acceptable salt, polymorph, ester or hydrate thereof and/or pharmaceutically acceptable excipients wherein the invention is preferably devoid of an alkyl aryl polyether alcohol type polymer such as tyloxapol, a polyethylene glycol fatty acid ester such as polyethylene glycol monostearate and BAC. Also the present invention is preferably devoid of antioxidants such as sulfite but not limited to sodium sulfite, potassium sulfite and the like. The present invention also provides for a method for treating ocular inflammation and pain, e.g., after cataract surgery, wherein the method comprises topical application of a formulation according to the present invention to the eye of a patient in need thereof.
摘要:
The present application provides parenteral compositions of diclofenac or its pharmaceutically acceptable salt and methods for making and using such compositions. Some of the compositions of the present application has one or more following properties: (1) ready to be injectable, (2) in the form of an oil-in-water emulsion, (3) stable under appropriate storage conditions, (4) containing therapeutically effective amount of diclofenac or its pharmaceutically acceptable salt, (5) sterilizable by filtration (6) containing components acceptable by regulatory agencies (e.g. the FDA), (7) containing low oil content and thus not exacerbating hyerlipidemia, and (8) is neither hyperallergenic nor vein irritating.
摘要:
Данное изобретение относится к неизвестным ранее (3R,4R,5S)-4-Амино-5-(2,2-дифторацетиламино)-3-(1-этилпропокси)-циклогекс-1-енкарбоновой кислоте и ее эфирам, общей формулы 1, или их фармацевтически приемлемым солям, кристаллическим формам и/или гидратам, которые представляют интерес в качестве лекарственных субстанций для создания новых препаратов, предназначенных для профилактики и лечения гриппа, к способам их получения и применения, где R представляет собой водород, C 1 -C 3 алкил.