Roberto Abadie’s (2010) book, The Professional Guinea Pig: Big Pharma and the Risky World of Human Subjects, brings up many ethical issues. Abadie’s enquiry illustrates matters of beneficence, respect for autonomy, and non-maleficence the in pharmaceutical research environment. In the book, Abadie examines the pharmaceutical phase I clinical research and HIV trials from the perspective of trial participants. The majority of Abadie’s narrative focuses on professional guinea pigs. Professional guinea pigs are trial participants that take part in multiple pharmaceutical trials as a way to make a living or to accommodate their chosen lifestyle. After examining the book, the reader can raise questions concerning these principles. Seemingly, the …show more content…
The outcomes new therapies produce may seem to justify and validate the means of over compensating subjects. Some may also contend that the benefit outweighs the harm, and the aim is to produce a net benefit over harm when considering beneficence and non-maleficence together (Gillon, 1994). Nevertheless, there is no obligation of beneficence to others, but there is an obligation not to harm (Gillon, 1994). The former utilitarian statement’s intentions appear virtuous, however, the true means the industry uses and their intent is flawed. Trouiller and colleagues’ (2002) evidence supports the claim that the pharmaceutical industry’s intent is to profit from research given their reluctance to develop new therapies that would help millions due to costs and risk of investment. Consequently, subjects are then merely a means. Given this, it seems relevant to consider a deontological perspective. When the intent of the research is to produce therapies for profit, the intent ignores the social duty to help and only benefits a few. Moreover, when intention is to profit, people become means and not the ends. Kant expressed that people should always be treated as ends and not only means (Munson, 2012). The practice of using humans as tools, seemingly, is a dehumanizing practice and in itself harmful. Accordingly, the intentions reinforcing the guidelines and practices of the pharmaceutical industry undermine the principle of
A new oral pharmaceutical drug for type- two diabetes had been approved for clinical use, it was called Compound 17392. Marketing companies instantly wanted to have prescribers adopt and sell the product and researchers wanted to further investigate previous reports of liver toxicity in patients. Now since paying patients to try new pharmaceutical drugs was an issue due to it appearing to interfere with clinical judgement and upholding the duty to do what is best for the patient, a new idea of furthering research for the drug came into play. The idea included recruiting a group of physicians who were in the top ten percent of prescribers for type-two diabetes. Following regulations put in place by researchers, these physicians were to enter eligible patients into the trial for Compound
I agree with these conclusions because you can see them throughout history and in modern society. While the book mostly went
Why not all agree, as you can all read the book?” Therefore, he questions the diverse kinds of
This source is useful by means of kindly explaining how people find the book inappropriate. In addition to explaining the other side, the article provides evidence showing how
Growing up in Australia can have a positive effect the students, however, many suffer from discrimination, isolation and racism. This is practically hard for children to endure as the as told by Hop Dac and Aditi Gouvernel. Dac and Gouvernel are both from Asian backgrounds in their memoirs "Pigs From Home" and "Wei Li and Me". Both of these memoirs clearly convey that the struggled with going up in Australia. Gouvernel faced issues with being different from the rest of the students and Dac found it difficult to accept the lifestyle and culture of his grandmother.
In contrast to this viewpoint, an article and associated editorial in the New England Journal of Medicine in May 2015 emphasized the importance of pharmaceutical industry-physician interactions for the development of novel treatments, and argued that moral outrage over industry malfeasance had unjustifiably led many to overemphasize the problems created by financial conflicts of interest. In 2009 a study found that "a number of academic institutions" do not have clear guidelines for relationships between Institutional Review Boards and industry. The influence of the pharmaceutical industry on medical research has been a major cause for
Likewise, the best treatment should not refer to local treatment standards, but the best standards available to maximize the beneficence and justice applied to participants already undertaking the burden of participating in a clinical trial. Unfortunately, ethical principles can sometimes be neglected due to competition in the field and the increase of regulations. This has resulted in some ethically questionable trials based in third world countries that violate justice, autonomy, and beneficence to obtain faster results. Harold Varmus and David Satcher’s perspective on what standards and guidelines should be implemented in clinical trials in third world countries differs from that of Angell’s arguments. They make the argument that compared to other approaches, a placebo is the most justified way to obtain clear and rapid results from clinical trials regardless of what treatments may currently be available.
In this paper, I will be making an argument about why animal testing is a good thing for humans to have for the sake of products. Animal testing has caused a great relief of pain and suffering to humans. It has been the foundation of humans finding curves for diseases and then being able to treat those diseases. Animal testing makes it possible for humans to develop new drugs and vaccines. Personally, I stand for the use of animal testing as a beneficiary of science and human products.
Methodology This chapter will discuss how we use our methods as a tool to answer the research question and working questions. The chapter will include ontological considerations as well as a reflection of our epistemological standpoint in order to evaluate how ‘knowledge’ is obtained about the DSM and pharmaceutical companies and to what extent the issues are based on assumptions or available empirical data. An overview of our research design and considerations behind our data collection will be included too. Furthermore, it will include a literature review where literature on this topic is examined. It will include literature on the DSM, where conflicts of interest and public policies regarding disclosure of ethical issues as one example
Research has further assisted in the development of drugs such as insulin and penicillin. It was said in the beginning that animals would never feel pain while going through such experiments, but there have been many times where labs go against that assumption. In some labs, the aftermath of the experiments are so immoral, it’s impossible for one to think what that animal endured. As of today, labs across the world are trying to enforce the 3Rs, which are replacement, reduction, and refinement. The 3Rs is a campaign who hopes to replace animals with non-living models, reduce the number of animals begin used, and finally refine the practice of using animals according to Hajar.
Introduction In this essay, I will be comparing Deontology to Utilitarianism. I will attempt to substantiate why I am justified in arguing that Deontology is a superior moral theory than Utilitarianism. A Discussion of the Main Elements of Utilitarianism Utilitarianism is a moral theory developed by English philosopher Jeremy Bentham (1947 – 1832) and refined by fellow countryman John Stuart Mill (1806 – 1873).
Furthermore, as Sieber and Tolich (2012) warn, in case there are any potential risks assumed, the researcher should think of the benefits the research can bring to the field (p. 22), and they define these benefits as “desirable outcomes for subjects and the community” (p. 23). Therefore, to some extent, the researcher has to compensate for the potential risks by ensuring that the research results will somehow contribute to the subject, or will ameliorate the current situation in the community or the context, and these benefits
Imagine an enraged animal rights activist charging toward a scientist in a white lab coat, desperate to free the little mice that are being used as test subjects. Although comical, this scene may be quite accurate when describing the passion that animal lovers have when it comes to the touchy subject of animal testing. For centuries, animal testing has been used in the medical research field, however many are now beginning to question whether it is ethical. Millions of animals are killed per year due to animal testing, so is this practice worth banning? Animal testing is a controversial subject, with supporters pointing out the medical advances that have stemmed from animal research and animal rights activists declaring it cruel and immoral.
Mini Pig Cost: 250-1,5K Rarity: Not too Rare Mini pigs are pigs that have been selectively downsized over many generations in order to produce a pig that stays small, and can therefore make a great indoor pet. A mini pig will generally grow 12-16 inches and will reach 25-65 pounds; similar to a smaller dog. Mini pigs need a lot of attention; they do best with a companion pig to keep them company. They work well for people with allergies because they have coarse hair, called bristles, rather than fur.