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1.
Indian J Physiol Pharmacol ; 2013 Jul-Sept; 57(3): 293-307
Article de Anglais | IMSEAR | ID: sea-152610

RÉSUMÉ

Objectives : 1. To compare the percentage of patients that reach target LDL-C goals with 10 mg Vs. 20 mg of atorvastatin as a starting dose. 2. To compare Health Related Quality of Life (HRQOL) in patients on 10 mg Vs. 20 mg of atorvastatin. Methods : A prospective, double blind, parallel groups, unicentric study of patients of dyslipidemia, randomized to receive atorvastatin 10 mg (n=75) or atorvastatin 20 mg (n=75) once daily for 12 weeks. Safety reporting of incidence of adverse events was done. Results : Significantly more number of patients (P<0.05) reached target LDL-C levels at the end of 12 weeks in the 20 mg group (77.27% in the high risk group, 100% in moderately high risk group and 100% in the moderate risk group) when compared to 10 mg group (32% in the high risk group, 75% in moderately high risk group and 83.33% in the moderate risk group). Increase in HRQOL at the end of 12 weeks was also significantly greater (P<0.001) in 20 mg group (27.89%) vs. 10 mg group (19.26%). Conclusions : Selecting the starting dose of atorvastatin according to the patients risk category (by using the Framingham’s algorithm for calculating cardiovascular risk) and the percentage reduction in LDL required, will result in greater success in achieving LDL goals and better quality of life.

2.
Indian J Physiol Pharmacol ; 1997 Apr; 41(2): 144-8
Article de Anglais | IMSEAR | ID: sea-106399

RÉSUMÉ

Some of the chromophoric chain substituted hemicyaninocolourants (CCHCs) were synthesized and confirmed on the basis of nitrogen analysis. These were tested for their antinociceptive activity in albino rats against tail flick technique and sodium chloride induced writhing test. Test compounds were given in graded doses (10, 20 and 50 mg/kg, intraperitoneally) and compared with morphine and aspirin as standard controls. Two compounds CCHC-1 and CCHC-2 showed antinociceptive activity in a dose-dependent manner in both the experimental models. The compound CCHC-3 did not exhibit antinociceptive activity to any significant extent.


Sujet(s)
Analgésiques/administration et posologie , Analgésiques morphiniques , Animaux , Anti-inflammatoires non stéroïdiens/administration et posologie , Acide acétylsalicylique/administration et posologie , Agents colorants/administration et posologie , Cyclohexylamines/administration et posologie , Relation dose-effet des médicaments , Femelle , Injections péritoneales , Mâle , Morphine/administration et posologie , Azote/analyse , Douleur/induit chimiquement , Quinoléines/administration et posologie , Rats , Rat Wistar , Normes de référence , Chlorure de sodium/administration et posologie , Relation structure-activité , Queue
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