1. A solid dosage composition comprising at least one pharmaceutically active ingredient and at least one controlled release agent, wherein the immediate release profile of the at least one pharmaceutically active ingredient is controlled by the apparent viscosity of the controlled release agent, and where at least one pharmaceutically active ingredient wet granulated. 2. A method of manufacturing a solid dosage composition containing at least one pharmaceutically active ingredient and at least one controlled release agent, wherein the immediate release profile of the at least one pharmaceutically active ingredient is controlled by the apparent viscosity of the controlled release agent, and where at least one pharmaceutically active ingredient wet granulated. 3. A solid dosage composition containing at least one pharmaceutically active ingredient and at least one controlled release agent, where the apparent viscosity of the controlled release agent is from 100 to 100,000 cP and where at least one pharmaceutically active ingredient is wet granulated. 4. The solid dosage composition according to claim 3, wherein at least one of the pharmaceutically active ingredients is ibuprofen. The solid dosage composition according to claim 3, wherein at least one of the controlled release agents is hydroxypropyl methylcellulose. The solid dosage composition according to claim 3, where at least one of the agents1. Твердая дозированная композиция, содержащая по меньшей мере один фармацевтически активный ингредиент и по меньшей мере один агент контролируемого высвобождения, где профиль немедленного высвобождения по меньшей мере одного фармацевтически активного ингредиента регулируется кажущейся вязкостью агента контролируемого высвобождения, и где по меньшей мере один фармацевтически активный ингредиент подвергнут влажному гранулированию.2. Способ изготовления твердой дозированной композиции, содержащей по меньшей мере один фармацевтически активный ингредиент и по меньшей мере один
