[1]
|
G. Sanz and V. Fuster, “Fixed-Dose Combination Therapy and Secondary Cardiovascular Prevention: Rationale, Selection of Drugs and Target Population,” Nature Clin-ical Practice Cardiovascular Medicine, Vol. 6, No. 2, 2009), pp. 101-110. doi:10.1038/ncpcardio1419
|
[2]
|
“Global Burden of Disease 2004 Update,” World Health Organization, 2008.
|
[3]
|
C. D. Mathers and D. Loncar, “Projections of Global Mortality and Burden of Disease from 2002 to 2030,” PLoS Medicine, Vol. 3, No. 11, 2006, p. e442.
doi:10.1371/journal.pmed.0030442
|
[4]
|
M. R. Law and N. J. Wald, “Risk Factor Thresholds: Their Existence under Scrutiny,” British Medical Journal, Vol. 324, No. 7353, 2002, pp. 570-576.
doi:10.1136/bmj.324.7353.1570
|
[5]
|
V. Kumar, R. P. Shah and S. Singh, “LC and LC–MS Methods for the Investigation of Polypills for the Treat-ment of Cardiovascular Diseases: Part.1 Separation of Active Compo,” Journal of Pharmaceutical and Biomed-ical Analysis, Vol. 47, 2008, pp. 508-515.
doi:10.1016/j.jpba.2008.01.041
|
[6]
|
S. P. Clissold, “Aspirin and Related Derivatives of Sali-cylic Acid,” Drugs, Vol. 32, 1986, pp. 8-26.
doi:10.2165/00003495-198600324-00003
|
[7]
|
D. G. Julian, D. A. Chamberlain and S. J. Pocock, “A Comparison of Aspirin and Anticoagulation Following Thrombolysis for Myocardial Infarction (the AFTER Study): A Multicentre Unblinded Randomized Clinical Trial,” BMJ (British Medical Journal), Vol. 313, No. 7070, 1996, pp. 1429-1431.
|
[8]
|
J. W. Nawrocki, S. R. Weiss, M. H. Davidson, D. L. Sprecher, S. L. Schwartz, P. J. Lupien, P. H. Jones, H. E. Haber, et al., “Reduction of LDL Cholesterol by 25% to 60% in Patients with Primary Hypercholesterolemia by Atorvastatin, a New HMG-CoA Reductase Inhibitor,” Arteriosclerosis, Thrombosis, and Vascular Biology, Vol. 15, No. 5, May 1995, pp. 678-682.
doi:10.1161/01.ATV.15.5.678
|
[9]
|
L. Pilot, M. Abrahamowicz, M. Eisenberg, K. Humphries, H. Behlouli and J. V. Tu, “Effect of Different Angioten-sin-Converting-Enzyme Inhibitors on Mortality among Elderly Patients with Congestive Heart Failure,” Canadian Medical Association Journal, Vol. 178, No. 10, 2008, pp. 1303-1311. doi:10.1503/cmaj.060068
|
[10]
|
Q. Zhang, H. Jin, L. Wang, J. Chen, C. Tang and J. Du, “Randomized Comparison of Metoprolol Versus Con-ventional Treatment in Preventing Recurrence of Vaso-vagal Syncope in Children and Adolescents,” International Medical Journal of Experimental and Clinical Research, Vol. 14, No. 4, pp. 199-203.
|
[11]
|
E. R. Montgomery, S. Taylor, J. Segretario, et al., “De-velopment and Validation of a Reversed-Phase Liquid Chromatographic Method for Analysis of Aspirin and Warfarin in a Combination Tablet Formulation,” Journal of Pharmaceutical and Biomedical Analysis, Vol. 15, No. 1, 1996, pp. 73-82.
|
[12]
|
S. Erturk, A. E. Sevinc, L. Ersoy and S. Ficicioglu, “HPLC Method for the Determination of Atorvastatin and Its Impurities in Bulk Drug and Tablets,” Journal of Pharmaceutical and Biomedical Analysis, Vol. 33, No. 5, 2003, pp. 1017-1023.
doi:10.1016/S0731-7085(03)00408-4
|
[13]
|
A. Puratchikody, R. Valarmathy and P. Shiju, “RP-HPLC Determination of Atorvastatin Calcium in Solid Dosage Forms,” Journal of Pharmacological Reviews, 2003, pp. 79-80.
|
[14]
|
H. J. Panchal, B. N. Suhagia, N. J. Patel, I. S. Rathod, B. H. Patel, “Development and Validation of a HPTLC Me-thod for the Simultaneous Estimation of Atorvastatin Calcium and Ezetimibe,” Chromatographia, Vol. 69, No. 1-2, 2009, pp. 91-95. doi:10.1365/s10337-008-0831-z
|
[15]
|
F. Belal, I. A. Al-Zaagi, E. A. Gadkariem and M. A. Ab-ounassif, “A Stability-Indicating LC Method for the Si-multaneous Determination of Ramipril and Hydrochloro-thiazide in Dosage Forms,” Journal of Pharmaceutical and Biomedical Analysis, Vol. 24, No. 3, 2001, pp. 335-342. doi:10.1016/S0731-7085(00)00474-X
|
[16]
|
M. B. Shankar, F. A. Metha, K. K. Bhatt, R. S. Metha and M. Geetha, “Simultaneous spectrophotometric determi-nation of losartan potassium and hydrochlorothiazide in tablets,” Indian Journal of Pharmaceutical Sciences, Vol. 65, No. 2, 2003, pp. 167-170.
|
[17]
|
“ICH Stability Testing of New Drug Substances and Products Q1A (R2),” International Conference on Har-monization, IFPMA, Geneva, 2003.
|
[18]
|
“ICH guidelines on Validation of Analytical Procedures, Text and Methodology Q2 (R1),” FDA, Published in the Federal Register 60, 1995.
|
[19]
|
“United States Pharmacopoeia,” 32nd Edition, United States Pharmacopeial Convention, Rockville, USP 32, 2009.
|
[20]
|
M. Bakshi and S. Singh, “Development of Validated Stability-Indicating Assay Methods-Critical Review,” Journal of Pharmaceutical and Biomedical Analysis, Vol. 28, 2002, pp. 1011-1040.
|