Wednesday, May 6, 2020

FDAs Approval of Prescription Drugs Essay - 1536 Words

There are many direct to consumer advertising for prescription drugs. On television, magazines, radio etc, you see the most recent advertisements for prescription drugs. After some people see the advertisements they soon rush over to their doctor and their illness and life would be perfectly pain and stress free. Making the public conscious of options for treatment is not a bad thing. But these false advertisements are misleading consumers onto unnecessary treatment. Advertisements have one primary purpose that is to persuade. Prescription medications Ads tell the consumers to get treatment and also imply that they have the need for it to solve their problems. Since prescription Ads have been introduced, the pharmaceutical†¦show more content†¦Merck will soon face many challenges in the business of producing drugs. The companys most popular drugs are coming to a close to their patent expiration. One of the best selling drugs is called Zocar, which is used for cholest erol problems. Zocar will have to soon face competition next June from other generic drug makers. The elimination of Zocar from the market will erase the $5.2 billion sales annually. Fosomax, an osteoporosis relieving drug, produced by Merck will soon lose the$ 2.2 billion annual sales because of the expiration of its patent. Also, another problem is the struggles recently to find new medicines. The prescription painkiller drug, which was introduced in 1999, is called Vioxx. Vioxx was introduced by Merck and co. Vioxx served the purpose of being a painkiller in the relief of osteoarthritis, rheumatoid arthritis, painful menstruation and other types of acute pain. This painkilling drug would be classified as a non-inflammatory drug (NSAIDs). Last year, in September 2004, Merck withdrawed Vioxx, off the market. Studies of Vioxx showed that it doubled the risk of a heart attack or stroke for patients who have used it more than 18 months. After Merck, withdrawed Vioxx fr om the market, the FDA, issued a public health advisory for the users of Vioxx. Therefore, Vioxx was on the market for five years withoutShow MoreRelatedThe Food And Drug Administration1204 Words   |  5 PagesThe Food and Drug Administration (FDA) is best known for its role on protecting the health of the public by making sure that food, medications are safe and effective. Especially when it comes to the pharmaceutical industry, its mission is to regulate pharmaceutical manufacturers, as well as the drug approval process. However, in the recent years, many arguments and controversy regarding drug development and regulation have risen. Drug advertisements make false and misleading claims, products areRead MoreThe Drug Of Medical Marijuana983 Words   |  4 Pagescan be. Likewise, drug companies would obviously prefer a system in which consumers face potential jail time for marijuana and forced to pay sky high prices from prescription drugs which synthesize marijuana’s c hemicals. There is also revolving door between employees of drug companies and the FDA, another obvious conflict of interest. However, there are larger systematic conflicts of interest within the FDA. In 1992, Congress passed the Prescription Drug User Fee Act allowing drug companies to payRead MoreThe Drug Advertisements Of New Zealand992 Words   |  4 PagesBill Maher once mocked the aggressive nature of the drug advertisements that direct you to tell your doctor that their drug is right for you. â€Å"Tell your doctor? Shouldn’t your doctor tell you what drugs you need. When you tell your doctor isn’t he just a dealer at that point,† said Bill Maher. The American public generally trusts their government to protect them from the hidden dangers prescription and over-the-counter drugs. However, that trust isn’t fully warranted as the FDA has been featuredRead MoreRegulatory Agency: Food and Drug Administration Essay1617 Words   |  7 PagesRegulatory Agency: Fo od and Drug Administration Victoria Steele University of Phoenix Regulatory Agency: Food and Drug Administration The regulation of all areas of health care in The United States falls to The United States Department of Health and Human. One such area is the regulation on medications dispensed within the United States. The section of The United States Department of Health and Human Services responsible for regulation on medications is the Food and Drug Administration (FDA)Read MoreThe Food And Drug Administration Is A Regulatory Agency Responsible For The Public Health Of American Residents Essay1800 Words   |  8 PagesThe Food and Drug Administration is a regulatory agency responsible for the public health of American residents. The agency is located in Silver Springs, Maryland. The current extent of FDA regulations reaches a wide variety of product groups such as electronic devices, cosmetics, foods, biologics, tobacco, medical devices, and veterinary devices (US Food Drug Administration, 2016). The FDA is also accountable for the safety of the food supply, prescription drugs, and th e manufacturing of productsRead MoreThe Politics and Economics of FDA Drug Approval Essay2413 Words   |  10 PagesEconomics of FDA Drug Approval The United Sates Food and Drug Administration has been protecting American consumers for around 70 years. The FDA assures the safety drugs, medical devices, chemicals, cosmetics, foods and additives by evaluating products for approval. Controversy has recently been surrounding the FDAs drug approval process, due to a general trend to get pharmaceuticals on the market more quickly. The FDA has been under pressure from congress and the public to speed approval, but pharmaceuticalRead MoreEnsuring Consumer Safety: Toward Redefining the U.S. Food and Drug Administration4116 Words   |  17 Pagesthe U.S. Food and Drug Administration The Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services. The FDA is responsible for protecting and promoting public health through the regulation and supervision of foods, medical devices, and prescription and over-the-counter pharmaceutical drugs (medications). The FDA regulates and supervises medical devices and drugs throughout their development, manufacturing, process of approval, marketing, and postRead MoreShould Drugs Be Safe For Consumption?1688 Words   |  7 Pagesthese medications will benefit your health? How do you know that the drugs are safe for you? Every day, men and women enter hospitals because of a doctor’s appointment or because of an infirmity. Most of them will have prescribed drugs from doctors, but none of them will question of the effectiveness and safety of the pharmaceuticals. There are also many other ways to obtain drugs like through a local drug store, but the drugs are considered to be s afe for consumption. This is because the UnitedRead MoreRace Labeling Of Non Whites From Clinical Trials1656 Words   |  7 Pagesbroader goal of increasing racial minorities’ participation in clinical trials (Winickoff and Obasogie, 2008). For instance, by specifying African Americans as the only beneficiaries of BiDil, the same idea could be applied for a special efficacy drug for Whites, â€Å"the largest and most lucrative population segment of the United States† (Winickoff and Obasogie,2008). This logic could be used to justify the exclusion of non-Whites from clinical trials. This seems to be what happened in 2006 when Schering-Plough

No comments:

Post a Comment

Note: Only a member of this blog may post a comment.