The Pharmaceutical drug companies have a tendency to focus more on the sales and revenue than the research of any given product. This trend leads to misrepresentation of crucial scientific research on products. “A wide variety of research practices has been described as being used to distort the medical literature in favor of a clinical trial sponsor’s pharmaceutical intervention,” (Ross, Gross, & Krumholz, 2012, para. ).But also, not only do the drug companies practice unethical research studies, they spend money pushing products and incentives to physicians for writing the prescriptions for those drugs. That monetary value of those incentives is, often, more than the research on the drug itself. Two companies have been accused, tried, and charged for smudging results and falsifying findings for their benefit. It appears that pharmaceutical companies have interchanged the quest of treating and healing sickness and disease with the sole purpose of making money.…
d. Ensure that customers and medical specialists are given enough info about prescription drugs on branding and marketing IV. The chosen medical goods or services classification a. Drug Advertising, Branding and Publicity V. Reason for selecting this section a. The DDMAC division of the FDA is accountable for regulating conformity in advertising, branding and public relations. b. The DDMAC is accountable for proficient healthcare promotional procedures for direct-to-consumers advertising c. Info is given as well as what may or may not be included in end-user copies. VI. Conclusion a. Associate the significance of FDA regulations on drugs with existing measures…
The 2010 edition replaces all previous editions of the Pharmacist’s Manual issued by the Drug…
PROCEDURAL HISTORY: Section 503A of the Food, Drug and Cosmetic Act, 21 U.S.C. § 353a exempts compounded drugs from certain provisions of the Food and Drug Administration’s standard approval requirements; provided that the distributors abide by certain restrictions, including advertising and promoting selected compounded drugs. The Act, however, did not prohibit the advertising of its effectiveness. The Central Hudson Gas et. Elec. Corp v. Public Serv. Comm’n of NY, 447 U.S. 557, 566 held that the restrictions directly advance its interests, or that less restrictive alternatives were unavailable.…
DTCPA can interfere by encouraging patients to request an inappropriate drug. When a doctor declines to write a prescription for the requested medicine, it can lead to patients questioning the qualifications of the physician. This has a negative impact and is shown increase patient switching of physicians due to the decrease in their satisfaction. With this in doctor’s minds, it can lead to pressure to prescribe the wrong medicine simply because it was asked for. Unnecessary interference of a doctor-patient relationship could be eliminated with the removal of…
“We Love Them. We Hate Them. We Take Them.” by Abigail Zuger discusses the sensitive topic of prescription drug abuse by doctors. She claims in her essay that drug advertisements have become so persuasive and aggressive, that doctors are feeling the need to prescribe them to patients, even though they don’t necessarily need them. Zuger uses a personal experience from her life to illustrate her thesis for the audience. The experience was when she prescribed one of her patients a pill because she felt it would help him, and she continually told him to keep taking it, but he told her it made him feel the opposite of better. She still pursued him to take it even though his body was signaling for him not to. He ended up in the hospital from this drug, and she feels awful about the entire situation. Zuger claims the situation has opened her eyes to the real effects of prescription drugs and to listen to the patient’s body, the description of the drug. “Beware of Drug Sales” by Therese Cherry claims that prescription and over-the-counter drugs are being too aggressively advertised, persuading people who don’t even need them to take them. She claims even some doctors are persuaded by the ads to prescribe them to their patients (such as Zuger), some are even paid. She claims this is an extremely negative effect on our…
1. Should certain kinds of ads be banned in the interest of health/morality – alcohol, cigarettes, and prescription meds?…
Going to the doctor’s office is never a fun experience. Probing, poking, and trying to decipher what the doc writes on your prescription can be confusing, however, the most upsetting part is what goes on behind closed doors. Big Pharma, chapter 3 of Lies the Media Tells Us, explains the PR tactics of drug companies. James Winter explains these tactics used to persuade doctors to use their brand. In some cases these doctors can get free vacations, cars, front row seating for a basketball game, and a stack of cash. The doctors that respond to these tactics are completely unethical. Doctors have the responsibility to prescribe the best drugs for their patients. Although many Doctors pick what gives the best gift package.…
The role and responsibility of the U.S. Food and Drug Administration (FDA), most importantly, is to uphold the laws dictated by the government concerning products that include drugs, medical products, food, and non-health related products and to protect and promote public health across the country. This essay focuses on several aspects of the FDA, from the role of the agency and its effect on health care in the United States, to the authority this agency carries in relation to health care. There will also be an explanation of how the FDA carries out these responsibilities on a day-to-day basis. The FDA has held a strong presence in the realm of public health since 1848 when it began as a consumer protection agency (FDA, 2013). The FDA, formed after the 1906 Pure Food and Drug Act was put in place and inspired by the scientific work of Harvey Washington Wiley, who was the Chief Chemist at the U.S. Department of Agriculture. Wiley worked to eliminate the dangerous practices of marketing unregulated drugs and food products to consumers (FDA, 2013). Since that time, the FDA has become a powerful force, monitoring and working to protect public health in the United States.…
Another reason that DTC advertisements need stricter regulations is because the advertisements mislead consumers with distorted information about drugs. Furthermore, as DTC advertisements give consumers the wrong perspective, consumers would expect false consequences. These false consequences sometimes turn out to be a placebo effect. However, the problem is that placebo effect requires many random circumstances to be triggered, such as doctors and devices (Almasi et al. 284). Therefore, it is hard to expect for all patients to generate a placebo effect. Moreover, these false expectations disrupt the physician-patient relationship because consumers who are educated by misleading advertisements would require alternative treatment…
Your standing in line at your local drug store, head killing you, your face feels like it’s ready to explode, and you cannot breathe if your life depended on it. In short your allergies are making your life unbearable, and you are completely out of Sudafed. When you finally arrive at the pharmacist and ask for a box, you are asked for your driver’s license and then promptly turned away. Recent laws have you waiting one more week before purchasing anything that contains pseudoephedrine or ephedrine. Disgruntled and in pain, you walk away and as you leave the store you overhear the cashier tell a customer “instead of buying a pack a day, why don’t you just buy a carton?” Right about now the FDA’s “…goal of a healthier, safer nation…” ("Overview Of The FDA Mission", 2007) does not feel so accurate. The FDA’s regulations are unjust, because they place corporate profits above consumers’ safety, ban proven natural beneficial health medications, and allow the public’s lifestyle demands to alter their mission.…
If I had to argue to my local community of Dayton, Ohio about the severity and effects of prescription drugs I would tell them this:…
The FDA helps advance public health by speeding up product innovations. The public is informed with science-based in, Puerto Rico formation needed to use medicines, foods and devices to improve their health ( UDHHS, 2010). The FDA approval process not only makes sure that the product's ingredients are safe but also that labels show all ingredients and do not make unverified claims. This has caused the FDA symbol to now become one that consumers trust(Gelinas, 2010).…
The current FDA protocol calls for pharmacies to be registered under the FDA and these pharmacies must get approval from the FDA to sell these drugs (Kindy and Sun 3). Even though the FDA approves the drugs, there is no way to monitor how many doctors are prescribing, In addition, the FDA was forced to change its rules because pharmacies were ordering drugs without the government’s consent (Tavernise 1). However, with the advancement of technology, patients should be required to undergo strict background checks, aimed at identifying those individuals who go from one doctor to another obtain additional prescription drugs. This will allow the FDA to identify drug abusers and assist them in finding the help they need to overcome addiction or dependency. With this drug monitoring program, doctors will be able to help reduce drugs abuses, saving the medical industry millions of dollars in medical costs associated with drug addicts and…
Prescription drugs are a critical part of the health care system and chronic patients who rely on medicines to keep them healthy. Unfortunately, drug costs in the United States are too high and continue to be raised routinely. The unsustainable drug costs put a severe burden on the health care system and ultimately the patients. Should the United States government do more to regulate the cost of prescription drugs? It is still a debatable question as it is evident throughout history that developments of the pharmaceutical industry and science have increased when Congress passed legislations that support the innovation being conducted in the lab including policies like the Orphan Drug Act, the Prescription Drug User Fee Act, and the Food and…