Development and validation of HPLC and UV spectrophotometric methods for the determination of lumiracoxib in tablets
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[1] M. S. Sangoi,et al. Determination of lumiracoxib by a validated stability-indicating MEKC method and identification of its degradation products by LC-ESI-MS studies. , 2011, Journal of separation science.
[2] R. Moskowitz,et al. Coxibs and NSAIDs--is the air any clearer? Perspectives from the OARSI/International COX-2 Study Group Workshop 2007. , 2007, Osteoarthritis and cartilage.
[3] P. Tugwell,et al. Gastrointestinal safety of cyclooxygenase-2 inhibitors: a Cochrane Collaboration systematic review. , 2007, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.
[4] Z. Radi,et al. Effects of cyclooxygenase inhibition on the gastrointestinal tract. , 2006, Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie.
[5] G. Geisslinger,et al. Different COX-independent effects of the COX-2 inhibitors etoricoxib and lumiracoxib. , 2006, Biochemical and biophysical research communications.
[6] Anna Georgieva,et al. Pharmacodynamic behaviour of the selective cyclooxygenase-2 inhibitor lumiracoxib in the lipopolysaccharide-stimulated rat air pouch model. , 2005, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[7] T. Schnitzer,et al. Comparison of lumiracoxib with naproxen and ibuprofen in the Therapeutic Arthritis Research and Gastrointestinal Event Trial (TARGET), cardiovascular outcomes: randomised controlled trial , 2004, The Lancet.
[8] T. Schnitzer,et al. Comparison of lumiracoxib with naproxen and ibuprofen in the Therapeutic Arthritis Research and Gastrointestinal Event Trial (TARGET), reduction in ulcer complications: randomised controlled trial , 2004, The Lancet.
[9] K. Lasseter,et al. No influence of moderate hepatic impairment on the pharmacokinetics of lumiracoxib, an oral COX-2 selective inhibitor. , 2004, Pharmacological research.
[10] T. Tsuchiya,et al. Role of direct cytotoxic effects of NSAIDs in the induction of gastric lesions. , 2004, Biochemical pharmacology.
[11] L. Laine,et al. Gastrointestinal health care resource utilization with chronic use of COX-2-specific inhibitors versus traditional NSAIDs. , 2003, Gastroenterology.
[12] L. Laine. Gastrointestinal effects of NSAIDs and coxibs. , 2003, Journal of pain and symptom management.
[13] G. Burmester,et al. Gastrointestinal toxic side effects of nonsteroidal anti-inflammatory drugs and cyclooxygenase-2-specific inhibitors. , 2001, The American journal of medicine.
[14] K. Rainsford. Profile and mechanisms of gastrointestinal and other side effects of nonsteroidal anti-inflammatory drugs (NSAIDs). , 1999, The American journal of medicine.
[15] F. Berenbaum. Osteoarthritis. Preface. , 2010, Baillière's Best Practice & Research : Clinical Rheumatology.
[16] R. Willburger,et al. P362 LUMIRACOXIB SHOWS COMPARABLE EFFICACY AND A FAVOURABLE BLOOD PRESSURE PROFILE COMPARED TO INDOMETHACIN FOR THE TREATMENT OF ACUTE FLARES OF GOUT , 2006 .
[17] C. Hawkey,et al. Gastrointestinal tolerability of lumiracoxib in patients with osteoarthritis and rheumatoid arthritis. , 2006, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.
[18] C. Kaeding,et al. The use of NSAIDs and nutritional supplements in athletes with osteoarthritis: prevalence, benefits, and consequences. , 2005, Clinics in sports medicine.
[19] G A Green,et al. Understanding NSAIDs: from aspirin to COX-2. , 2001, Clinical cornerstone.