Abstract: In a solid pharmaceutical preparation containing water-soluble salts of levothyroxine and/or liothyronine as active ingredients, the water activity of said pharmaceutical preparation is adjusted to values of below 0.4 and, preferably, 0.1 to 0.3, measured at room temperature.

Abstract: In a solid pharmaceutical preparation containing water-soluble salts of levothyroxine and/or liothyronine as active ingredients, the water activity of said pharmaceutical preparation is adjusted to values of below 0.4 and, preferably, 0.1 to 0.3, measured at room temperature.

Abstract: In a method for producing stable acetylsalicylic acid solutions with pharmaceutically acceptable non-aqueous organic solvents such as, e.g., dimethylisosorbide, propylene glycol or diethylene glycol monoethyl ether, 0.005-2% by weight of a cyclic acid imide and/or 0.005-2% by weight of a sulfaminic acid as well as, preferably, 1-40% by weight, based on the weight of the solution, of a compound of the general formula are added to the solution. In the general formula, R1 represents H, CH3 or C2H5, n=0 or 1, and R2 represents H or one or more lower alkyl, lower alkyloxy or lower alkenyl residues having 1 to 5 carbon atoms.

Abstract: Pharmaceutical preparation containing Nifedipin as the active substance together with a solution promoter, such as, for example, copolyvidon or polyvinylpyrrolidone and/or glycerol-polyethyleneglycoloxystearate, and with a solvent, such as, for example, alcohols, in particular ethanol, or polyalcohols, as well as, optionally propelling agent for spraying in form of individually doseable sprays for sublingual administration and additionally containing in the sprayable prepartion 0.5 to 30 percent by weight of benzyl alcohol.

Abstract: A pharmaceutical preparation contains an active ingredient added to polyalcohols, such as polyethylene and/or polyalkylene glycols and/or oxystearates of glycerine-polyethyleneglycol and/or partial fatty acid esters of sorbitan or polyhydroxyethylenesorbitan and/or polyvinylpyrrolidone and/or polyvinylalcohols and/or fatty alcohol ethers of polyhydroxyethylene or fatty acid ester of polyhydroxyethylene and/or condensates of polyhydroxyethylene-polyhydroxypropylene, and especially dissolved in nifedipine in a weight ratio between 1:2 and 1:25. The composition contains ethanol as well, in an amount ratio between 1:25 and 1:4 of nifedipine:ethanol and can be sprayed with a propeller gas.

Abstract: A sprayable pharmaceutical preparation available in doses in aerosol containers comprises an active ingredient dissolved in polyalkylene glycol, and/or polyethylene glycol, and/or fatty glycolic acid ester of glycerine-polyethylene such as glycerine-polyethyleneglycol oxyoleate and/or glycerine-polyethyleneglycol oxystearate, and/or partial fatty acid esters of sorbitol or polyhydroxyethylene sorbitol, and/or polyvinylpyrrolidones, and/or polyvinyl alcohols, and/or fatty alcohol ethers of polyhydroxyethylene or fatty acid esters of polyhydroxyethylene and/or condensates of polyhydroxyethylen-polyhydroxypropylene and/or propylene carbonate, mixed with ethanol, substituted if necessary at least partially with middle chain diglyceride and/or triglyceride of fatty acids, and with a pharmacologically acceptable propellant, in particular halogenated hydrocarbons.