Valdecoxib was manufactured and marketed under the brand nameBextra byG. D. Searle & Company as an anti-inflammatory arthritis drug.[3] It was approved by the United StatesFood and Drug Administration (FDA) on November 20, 2001, to treat arthritis and menstrual cramps,[4][5] and was available by prescription in tablet form until 2005 when the FDA requested that Pfizer withdraw Bextra from the American market.[6] The FDA cited "potential increased risk for serious cardiovascular (CV) adverse events," an "increased risk of serious skin reactions" and the "fact that Bextra has not been shown to offer any unique advantages over the other available NSAIDs."[6]
In 2009, Bextra was at the center of the "largest health-care fraud settlement and the largest criminal fine of any kind ever."[4][7] Pfizer paid a $2.3 billion civil and criminal fine.Pharmacia & Upjohn, a Pfizer subsidiary, violated the United StatesFood, Drug and Cosmetic Act for misbranding Bextra "with the intent to defraud or mislead."[3]
A water-soluble and injectableprodrug of valdecoxib,parecoxib, is marketed in theEuropean Union under the tradename Dynastat.
On April 7, 2005, Pfizer withdrew Bextra from the U.S. market on recommendation by the FDA, citing an increased risk ofheart attack andstroke and also the risk of a serious, sometimes fatal, skin reaction. This was a result of recent attention to prescription NSAIDs, such asMerck'sVioxx. Other reported side effects wereangina andStevens–Johnson syndrome.
Pfizer first acknowledged cardiovascular risks associated with Bextra in October 2004. TheAmerican Heart Association soon after was presented with a report indicating patients using Bextra while recovering from heart surgery were 2.19 times more likely to suffer a stroke or heart attack than those takingplacebos.
In a large study published inThe Journal of the American Medical Association in 2006, valdecoxib appeared less adverse for renal (kidney) disease and heart arrhythmia compared to Vioxx, but elevated renal risks were slightly suggested.[9]
On September 2, 2009, theUnited States Department of Justice fined Pfizer $2.3 billion after one of itssubsidiaries, Pharmacia & Upjohn Company, pleaded guilty to marketing four drugs, including Bextra, "with the intent to defraud or mislead."[10] Pharmacia & Upjohn admitted to criminal conduct in the promotion of Bextra, and agreed to pay the largest criminal fine ever imposed in the United States for any matter, $1.195 billion.[11] A former Pfizer district sales manager wasindicted and sentenced to home confinement for destroying documents regarding the illegal promotion of Bextra.[12][13] In addition, a regional manager pleaded guilty to distribution of a misbranded product, and was fined $75,000 and 24 months on probation.[14]
The remaining $1 billion of the fine were paid to resolve allegations under the civilFalse Claims Act case and is the largest civil fraud settlement against a pharmaceutical company. Six whistleblowers were awarded more than $102 million for their role in the investigation.[15] Former Pfizer sales representative John Kopchinski acted as aqui tam relator and filed a complaint in 2004 outlining the illegal conduct in the marketing of Bextra.[16] Kopchinski was awarded $51.5 million for his role in the case because the improper marketing of Bextra was the largest piece of the settlement at $1.8 billion.[17]
Several HPLC-UV methods[18] have been reported for valdecoxib estimation in biological samples like human urine.[19][20] Valdecoxib has analytical methods for bioequivalence studies,[21][22] metabolite determination,[23][24][19] estimation of formulation,[25] and an HPTLC method for simultaneous estimation in tablet dosage form.[26]
^Sahu PK, Annapurna MM (2011).Analytical method development by liquid chromatography. Germany: LAP Lambert Academic Publisher.ISBN978-3-8443-2869-1.
^abZhang JY, Fast DM, Breau AP (February 2003). "Determination of valdecoxib and its metabolites in human urine by automated solid-phase extraction-liquid chromatography-tandem mass spectrometry".Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences.785 (1):123–134.doi:10.1016/s1570-0232(02)00863-2.PMID12535845.
^Sane RT, Menon S, Deshpande AY, Jain A (February 2005). "HPLC determination and pharmacokinetic study of valdecoxib in human plasma".Chromatographia.61 (3–4):137–41.doi:10.1365/s10337-004-0442-2.S2CID95275785.
^Mandal U, Jayakumar M, Ganesan M, Nandi S, Pal TK, Chakraborty MK, Roy Chowdhary A, Chattoraj TK (2004). "[title]".Indian Drugs.41: 59.
^Zhang JY, Fast DM, Breau AP (September 2003). "Development and validation of an automated SPE-LC-MS/MS assay for valdecoxib and its hydroxylated metabolite in human plasma".Journal of Pharmaceutical and Biomedical Analysis.33 (1):61–72.doi:10.1016/s0731-7085(03)00349-2.PMID12946532.
^Werner U, Werner D, Hinz B, Lambrecht C, Brune K (March 2005). "A liquid chromatography-mass spectrometry method for the quantification of both etoricoxib and valdecoxib in human plasma".Biomedical Chromatography.19 (2):113–118.doi:10.1002/bmc.423.PMID15473012.
^Sutariya VB, Rajashree M, Sankalia MG, Priti P (2004). "Spectrophotometric Estimation Of Valdecoxib In Pure Form And Tablets".Indian Journal of Pharmaceutical Sciences.66 (3):360–362.
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