StudentShare
Contact Us
Sign In / Sign Up for FREE
Search
Go to advanced search...
Free

FDA Should be Allowed to Regulate the Tobacco Industry - Coursework Example

Summary
"FDA Should be Allowed to Regulate the Tobacco Industry" paper draws its points is that FDA should be allowed to regulate the industry of tobacco. In the year 2000, the supreme court of the U.S.A ruled that FDA has limited authority to regulate tobacco use. …
Download full paper File format: .doc, available for editing
GRAB THE BEST PAPER92.2% of users find it useful
FDA Should be Allowed to Regulate the Tobacco Industry
Read Text Preview

Extract of sample "FDA Should be Allowed to Regulate the Tobacco Industry"

FDA Should be Allowed to Regulate the Tobacco Industry U.S.A Food and Drug Administration (FDA) is an agency which centers its purpose in regulatory, scientific and Public health and it monitors the accounting for every 25 cents of a U.S dollar used by consumers. It has a jurisdiction umbrella covering a wide range of food products (with the exception of poultry and meat), biological therapeutic agents, animal and human medicine, medical devices and so on. The agency was a U.S Department of Agriculture single chemist in 1862 and by 2001 it employed about 9,100 workers with a budget of about 1.3 Billion US dollars. Its employees comprise of pharmacologists, pharmacists, chemists, physicians, layers, veterinarians, microbiologists, among others. (Swann, 1998) This is a study aimed at answering the question, “Should or should not FDA be allowed to regulate the industry of tobacco?” Firstly, the answer from which the paper will draw its points is that FDA should be allowed to regulate the industry of tobacco. In the year 2000, the supreme court of U.S.A ruled that FDA has limited authority to regulate tobacco use. Thus, FDA doesn’t maintain anymore the children and tobacco part of their website. (FDA, 2000). But FDA’s mission stipulates very well that its responsibility to protect the health of the public through the ensuring of efficiency, security and safety of veterinary and human drugs, medical devices, biological products, US’s food supply, products that emit radiation and cosmetics. Thus, tobacco can be put under biological products. For instance, WHO defines tobacco products as those made of the tobacco leaf as the raw material, (either partially or their entirety). The intended purpose of these products is to suck, smoke, snuff or chew. Further, WHO cites various risks emanating from tobacco use like chronic diseases associated. Examples are; lung diseases, cancer as well as cardiovascular diseases. (WHO, 2009) FDA’s idea was based on smokeless products of tobacco and cigarettes which it defines as delivery devices of nicotine. Theirs was not a baseless assertion, but was lifted from several findings: (a) That effects of the use of nicotine and which are known by manufacturers of these products are addiction as well as other pharmacological impacts to consumers, (b) That these consumers utilize products made of tobacco to sustain their addiction, for weight loss and for mood –altering effect, (c) That the tobacco products manufacturers are aware that nicotine has effects that are pharmacological, (d) These manufacturers of tobacco products design them so as to provide to consumers with a nicotine dose, (e) Therefore, the consequence is that consumers continue utilizing smokeless tobacco and cigarettes to ensure sustainable of the nicotine addiction. The target of the campaign was especially to limit access to tobacco products by minors and also ban the advertising of cigarettes and the promotion aimed at adolescents. FDA also wanted tobacco manufacturers to be stopped from sponsoring sporting events and events of entertainment. (Stratton, 2001, p 127) Some merchants are notoriously known for selling tobacco products to minors. Sales laws in U.S.A are too much ignored even if they have been in the books for a while. However, it’s not a matter of ignoring a known fact on the part of merchants, but one of ignorance. Many of them aren’t aware of the prohibition. Efforts like those of FDA show that particular intervention on youth accessibility to tobacco products can do away with availability of tobacco commercially among minors. (Owing, 2005, p79) Further, in US today, advertisements for cigarettes are all over. A vast number of the US population is now addicted to cigarette smoking and they continue to ignore the dangers and the health issues related to tobacco smoking. According to Brown smoking of a10-pack cigarettes daily may cut a whole month from a person’s lifespan. He says this is a fact as per the findings of an organization’s research in its quest to study the effects of smoking tobacco. The research also found out that smoking has a negative impact especially on a person’s lungs and brain. The damages associated to smoking of tobacco to the lungs are; chronic predicaments like bronchitis and asthma, impotency due to harming of the system of reproduction, lung failure and coarse voice due to windpipe damage. Also it puts at risk the people who are not primarily smokers. This is called secondary smoking and it has been a leading course of about 10% of the ill effects associated with smoking. (Brown, 2008) The institute cancer says that tobacco smoking is associated with various cancerous diseases. These may include; chronic diseases of the lung, cardiovascular diseases and lung cancer. The statistics of 2007, according to their website, show that smoking of tobacco is a very big predicament in the US, which calls for regulation. Cigarette smoking is a leading cause of deaths in the US, yet it’s a preventable cause. It’s estimated that around 438,000 people die annually in the U.S.A due to tobacco smoking ill effects. Further more, secondary smoking leads to about 38,000 people’s demise per year in the United States. Lung cancer, which is one of the cancerous diseases highly associated with tobacco smoking, is the leading of all cancer deaths in US’s men and women. About 90% lung cancer deaths occur in males while in females it’s estimated that 80% lung cancer deaths result from smoking. Among cancerous diseases that are also attributed to tobacco smoking are the cancers of pancreas, mouth, throat, bladder, kidney as well as cervix. Also the population indulging in smoking is likely to have a heart attack, with a likelihood of six times more while compared with people who don’t smoke. The risk suffering of a heart attack also rises with the level of smoking. Despite there dangers involved, in the U.S.A, around 19.8% adults were tobacco smokers in the year 2007. U.S.A’s problem of smoking doesn’t end with adult tobacco smoking, but affects young people as well. By the term young people here put in mind the minors who smoke. About 23% of students in high school smoke and around 8% of students in the middle school also smoke and are current tobacco smokers in U.S.A (National Cancer Institute, 2007) While concluding, from these findings thus, FDA should be allowed to intervene in the tobacco industry. As a matter of fact intervention should not only focus on minors’ smoking of tobacco but also smoking in the whole population entirely. This is the only way the country can do away with the detrimental issues brought up by smoking like deaths, diseases and the high cost of health care. Work Cited: Brown J. Why You Should Quit Smoking Now. 2008. Retrieved February 25, 2009 http://www.associatedcontent.com/article/975354/why_you_should_quit_smoking_now.html?cat= 5 FDA, FDA and Tobacco Regulation. 2000. Retrieved February 25, 2009 http://www.fda.gov/opacom/campaigns/tobacco/default.htm National cancer institute. Tobacco Facts. 2007. Retrieved February 25, 2009 http://www.cancer.gov/cancertopics/smoking Owing, J.H. Focus on Smoking and Health Research. Nova Publishers, 2005. p 79. Stratton, K.R. Clearing the Smoke: Assessing the Science Base for Tobacco Harm Reduction. National. Academies Press, 2001. p 127. Swann, J.P. History of the FDA.1998. Retrieved February 25, 2009 http://www.fda.gov/search.html WHO. Tobacco. 2009. 2000. Retrieved February 25, 2009 http://www.who.int/topics/tobacco/en/ Read More

CHECK THESE SAMPLES OF FDA Should be Allowed to Regulate the Tobacco Industry

Tobacco Control Policy

The rest of this paper bases on the enormity of the tobacco epidemic.... This paper ''tobacco Control Policy'' tells us that there are over 1.... 5 billion tobacco smokers in the world at present.... tobacco consumption is the key source of unnecessary death worldwide and the main cause of avoidable death in developed countries.... At present, tobacco smoking is expected to kill over 10 million people per year by 2020....
15 Pages (3750 words) Research Paper

Training in Food Safety is Essential for Foodservice Employees

Employees in the foodservice industry continue to play an integral role in deterring the incidences of outbreaks of foodborne illnesses.... mployees in the foodservice industry are typically required to have sufficient knowledge of food safety Probable undesirable compounds found in foods span a broad range, from environmental contaminants such as dioxins and natural contaminants such as mycotoxins to agrichemicals such as pesticides.... Food safety is a crucial issue that engulfs the foodservice industry....
14 Pages (3500 words) Research Paper

Clinical Trial Drugs Regulations and Manufacture

For quite some time, clinical trials in the pharmaceutical industry have been regulated by several government bodies.... These regulations are set forth by entities like the United States Food and Drug Administration (fda), the European Medicines Agency (EMEA or EMA), the International Conference on Harmonization (ICH), and the Medicines and Healthcare products Regulatory Agency (MHRA), to name a few.... This law required new drugs be tested for safety before marketing, the results of which would be submitted to the fda in an NDA or New Drug Application....
42 Pages (10500 words) Thesis

Research Review on the FDA and the Regulation of Drugs

Moreover, the agency is also entitled to regulate various tobacco products in order to make sure that they comply with the set health standards.... fda is one of the government departments that contribute in enhancing the well-being of all citizens.... This paper provides detailed information about fda while trying to answer some of the most asked questions about the agency.... Introduction Food and Drug Administration (fda) is entitled to protect the American citizens' health....
7 Pages (1750 words) Research Paper

The Bureau of Alcohol and Firearms and Explosives

At the same time the FAA, also housed in the Department of Treasury, was responsible for collecting data, establishing license and permit requirements, and defining "the regulations that ensure an open, fair marketplace for the alcohol industry and the consumer (ATF online).... The paper "The Bureau of Alcohol and Firearms and Explosives" describes that balance is essential for an agency to work....
7 Pages (1750 words) Essay

Hookah Pen: The Latest Smoking Craze

An essay "Hookah Pen: The Latest Smoking Craze" claims that it has been determined that business entities are using these products to derive substantial profitability at times by misleading the users about inherent threat associated with such consumption.... ... ... ... In recent times, a huge change in smoking habit has been found among the young generation....
5 Pages (1250 words) Essay

Electronic Cigarettes

Federal and other state governments intend to ban sales of electronic cigarettes to minors and further propose approval for new products and inclusion of health warning labels as a way of taming the fast growing e-cigarette industry.... Electronic cigarette industry has thrived in the last few years and its success is based on many factors including the fact that it has successfully replaced the traditional cigarettes that is believed to be more harmful for consumption because of the high content of chemicals, odor, and tar....
17 Pages (4250 words) Essay

Clinical Trial Drugs Regulations and Manufacture

For quite some time, clinical trials in the pharmaceutical industry have been regulated by several government bodies.... From this work it is clear that the clinical trials should not adhere to strict guidelines, developers can be held accountable for their faults.... These regulations are set forth by entities like the United States Food and Drug Administration (fda), the European Medicines Agency (EMEA or EMA), the International Conference on Harmonization (ICH), and the Medicines and Healthcare products Regulatory Agency (MHRA), to name a few....
41 Pages (10250 words) Thesis
sponsored ads
We use cookies to create the best experience for you. Keep on browsing if you are OK with that, or find out how to manage cookies.
Contact Us