Pharmaceutical composition containing prasugrel and carvedilol, and purpose thereof
A technology of carvedilol phosphate and its composition, which is applied in the field of medicine, can solve the problems of unsustainable effect of prasugrel-like drugs, poor therapeutic effect, and single symptoms, and achieve the reduction of prasugrel resistance, Reduce the incidence of atherosclerosis and cardiovascular and cerebrovascular thrombosis events, and reduce the effect of toxic and side effects
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Embodiment 1
[0027] Example 1 Compound Prasugrel Carvedilol Tablets
[0028]
[0029] Preparation process: weigh the prescription amount of carvedilol, prasugrel, starch, dextrin and low-substituted hydroxypropyl cellulose and mix them evenly. Another suitable amount of 60% ethanol is added to the mixed powder, and the soft material is made after uniform mixing, which is granulated through a 16-mesh sieve and dried below 60°C. After drying, use an 18-mesh sieve to sizing, sieve out the fine powder in the dry granules, mix them with the sieved magnesium stearate, and then mix them with the dry granules evenly, press the tablet, and get it.
Embodiment 2
[0030] Example 2 Compound Prasugrel Carvedilol Tablets
[0031]
[0032] Preparation process: Weigh the prescribed amount of carvedilol, prasugrel, microcrystalline cellulose and hydroxypropyl cellulose and mix them evenly. Another suitable amount of 8% starch slurry solution is added to the mixed powder, mixed evenly to make soft material, granulated through a 16-mesh sieve, and dried below 60°C. After drying, use an 18-mesh sieve to sizing, sieve out the fine powder in the dry granules, mix them with the sieved magnesium stearate, and then mix them with the dry granules evenly, press the tablet, and get it.
Embodiment 3
[0033] Example 3 Compound Prasugrel Carvedilol Tablets
[0034]
[0035] Preparation process: weigh the prescription amount of carvedilol, prasugrel, starch, dextrin and low-substituted hydroxypropyl cellulose and mix them evenly. Another suitable amount of 60% ethanol is added to the mixed powder, and the soft material is made after uniform mixing, which is granulated through a 16-mesh sieve and dried below 60°C. After drying, use an 18-mesh sieve to sizing, sieve out the fine powder in the dry granules, mix them with the sieved magnesium stearate, and then mix them with the dry granules evenly, press the tablet, and get it.
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