The Food and Drug Administration, or FDA for short, is a government agency responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation, and by regulating the manufacture, marketing, and distribution of tobacco products. The FDA is also responsible for advancing the public health by helping to speed innovations that make medicines and foods more effective, safer, and more affordable; and helping the public get the accurate, science-based information they need to use medicines and foods, and to reduce tobacco use to improve health (About FDA 1). I am deeply concerned about how the FDA is regulating food. In my opinion, the FDA is failing miserably with their duties to the citizens of the United States of America. They appear to be more interested in profit than with the overall well being of the public. They are allowing people to consume dangerous amounts of fluoride. Studies have shown that food additives are causing serious health related issues. I feel that the FDA needs a massive overhaul in their top-level leadership positions in order for them to improve.…
risk, for drugs and medical devices, weighing risks against benefits is at the core of…
The FDA or Food and Drug administration is the oldest agency in the federal government of the U.S. This scientific, regulatory, and public health agency supervises items in the market that account for one fourth of every dollar spent by consumers. Earlier duties involved doing chemical analysis of farming products back in 1862 when it was known as the Department of Agriculture. In 1930 this department was renamed to the name that the public recognizes presently. The governing role started with the 1906 Pure Food and Drug Act, this law banned interstate trading in contaminated and incorrectly labeled food and drugs. The enforcement of this law was headed by Chief Chemist Harvey Washington Wiley. As of today, the agency now employs over 10,000 that is made up of pharmacists, physicians, veterinarians, lawyers, microbiologists, chemists and pharmacologists. These were the starting blocks of consumer protection that would later evolve in to the regulatory laws that we presently abide by. The responsibilities over the years have been modified, to keep up with changes in politics,…
Evaluation and Research,Center for Food Safety and Applied Nutrition, and National Center for Toxicological Research. This Agency was founded because of the Pure Food and Drug Act in 1906. The Pure Food and Drug Act was a law and it removed harmful foods and drugs. The responsibilities of the FDA was that it wanted to protect the public from harmful things that can harm the public. The FDA is an important part of the Federal Agency and the United States. The FDA is an important part of the federal government agency and United States.…
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). Whereas the FDA has many functions, such as regulation of food, cosmetics, tobacco, and animal medicine, one of the well-known functions of the FDA is pharmacy regulation. The FDA has a long history of ensuring public safety in relation to pharmaceutical medications.…
In the US, prescription medicine such as Vioxx were regulated by the Food and Drug Administration (FDA). Before a new drug could be sold in public, the manufacturer had to carry out clinical trials to demonstrate both safety and effectiveness. Advisory panels outside of the medical experts had to review the results of these trials to…
In 1999 the Food and Drug Administration (FDA) had approved Vioxx, what would become Merck’s “blockbuster” drug. Although the FDA had approved the drug there was uncertainty of the safety of drug. Vioxx was approved to treat a variety of conditions, such as osteoarthritis and acute pain, but there was also a chance that it would increase cardiovascular problems. What I found most interesting about this case was the changes in how drugs are brought to consumers, from how they are approved to how they are informed of the drug.…
I would be writing about interest groups and bureaucracy. The FDA bureaucracy article in a way stresses the importance or impact of the executive agency in carrying out its functions. I find testing how politicians try to sway the FDA (and other administrative agencies) in a way to suit their purpose is both necessary and may have a potential for undermining the administration. I thought the research question is of high importance; being able to test the efficiency (in terms of timeliness and quality of outcomes) of an administrative agency using the FDA as a case study. While different agencies will have their peculiarities, it is still necessary to be able to assess them this way. A drawback to this test could be something entirely unrelated…
The Food and Drug Administration (FDA) agency is the federal agency of the United States Department of Health and Human Services. FDA is responsible to protect public health by promising quality, efficacy, and safety of human and veterinary drugs, medical devices, food supply, cosmetics and any other products that release radiation (FDA Lecture PowerPoint). FDA is also responsible for assuring the security of food supply and its emerging effects on human health.…
The way I chose to use this small amount of information is to inform the reader of the tasks which the FDA claims to tackle. I focused specifically on the very first talking point about the protection of public health by assuring that foods are safe, sanitary, and properly labeled as I will be referring to sanitary and labels in the essay as well. This source, albeit short, was actually very helpful at introducing the reader to the talking points that will be covered throughout the paper and as a result the source was used fairly early into it. The first bullet was quoted to demonstrate to the reader that it seems that the FDA is a filter for us and prevents any products that deemed unsafe from food manufacturers. Which immediately leads to…
When it comes to the topic of prescription drugs being regulated, most of us will readily agree that this is a big concern for many Americans. Where this argument usually ends, however, is on the question of why do Americans pay some of the highest prices for prescription drugs compared to other countries. Whereas some are convinced that these high costs are set solely for the fact of the amount of money spent on producing these drugs, others maintain that there is an opportunity for medication prices to be regulated and also an opportunity to allow Medicare to negotiate with pharmaceuticals and possibly help bring down those high prices . I agree that prescription drugs should be regulated because there are many people that are victimized…
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).…
Some medications are not necessarily safe for humans even if it provides positive results in animals. In 950, there was a pill called the sleeping pill that caused 10,000 babies to be brought into this world with severe deformities which was tested prior to it’s commercial release. Another drug called Vioxx which is a arthritis medication showed that it provided a protective effect on an animal’s heart, yet the drug went on to cause more than 27,000 heart attacks and sudden cardiac deaths before it was finally pulled off the market. Rezulin or as some know it as troglitazone was approved by the FDA in 1997. The drug was intended to treat adult onset type 2 diabetes. Rezulin did indeed lower the blood sugar pressure in rats without negative effects, but later the animals reportedly began to have severe and sometimes fatal liver failure. The medication still hit the market and was not withdrawn until 2000 after it causes more than 400 deaths, but only because Los Angeles Times did an intensive investigation which caused them to change their label four times. Despite, all the drugs out there that has caused harm to humans animal testing still continues. Can you imagine all the drugs that could have helped the people in the world if we were actually able to get relevant results. Results that are actually beneficial and 100% guaranteed to work for humans. The percentage rate of a medication to actually been effective on humans is extremely low. 10% that is the percent we are suppose to rely on; the percentage that is used to predict a cure for diseases. Even the supposed animals that best replicate to us can still give us false results. For example, TGN1412 was tested on monkeys, rats, and rabbits and the results were positive for the medication to work, but in the human clinical trials, the subjects began to scream in agony. The drug was suppose to increase the immune responses to a virus, but instead it…
The speed of medical research together with drug companies race to create products has overtaken the system designed to keep people safe (Robert Davis par 2).…
federal government, the Food and Drug Administration is responsible for reviewing, approving and regulating medical products, including pharmaceutical drugs and medical devices. It also governs various other products, including food, cosmetics, veterinary drugs, radiation-emitting products, biological products and tobacco. The FDA protects the public health by assuring safety, effectiveness, quality, and security. Their responsibilities extend to the 50 United States, the District of Columbia, Puerto Rico, Guam, the Virgin Islands, American Samoa, and other U.S. territories and possessions ( FDA.gov Staff,…