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Merck is a multinational pharmaceutical company established in 1891. Merck researches, discovers, develops, manufactures and markets numerous vaccines and medicines through far-reaching programs that help deliver them to the people who need them.
Although Merck publishes unbiased, not necessarily the same biases used when preparing research (Bazerman, 2006), health information as a not-for-profit service, it appears that Merck misused data to delay the decision to withdrawal Vioxx.
It goes without question that Merck indeed successfully conducted research that gathered information related to the possible ill effects Vioxx may introduce. The controversy lays with their data analysis preparation techniques during the VIGOR (VIOXX Gastrointestinal Outcomes Research) & APPROVe (Adenomatous Polyp Prevention on VIOXX) studies (Sekaran, 2006).
The VIGOR study was primarily designed to examine the effects of Vioxx on side effects such as stomach ulcers and bleeding. The study did quantifiably show that patients prescribed Vioxx had fewer stomach ulcers and bleeding than patients on another drug but also revealed that there was a statistical increase in the number of cardiovascular events and stokes occurring in Vioxx patients (Kweder, 2004). But this was no great revelation. In 2001 an FDA advisory committee had to pass a vote to ensure that physicians were being informed of the VIGOR study findings (Kaiser, 2005).
APPROVe was a 156 week, 2600 person Vioxx vs. multi-centre, randomized, placebo-controlled double-blind quantitative study that investigated the side effects of Vioxx (Merck, 2004). APPROVe found that after 18 months of treatment, patients taking Vioxx had ...