Research Paper On Natural Drugs

The Food and Drug Administration (FDA) is a division of the Department of Health and Human Services (HHS) and received its name in 1930. Although the FDA’s roots can be traced back as far as 1862, its right as a regulatory agency came into effect under the 1906 Pure Food and Drugs Act. This legislation was created to eliminate misrepresentation of food and drugs in an effort to protect the health of the public. Over the years, the FDA’s role has further evolved to overseeing many areas other than just food and drugs. However, its mission has remained the same:

The Food and Drug Administration, also known as the FDA or USFDA, is responsible for protecting and advocating public health. They are the official government agency that ensures our drug supply is safe and effective. This is achieved through the regulation and supervision of food safety, dietary supplements, veterinary products, cosmetics, vaccines, biopharmaceuticals, medical devices, prescription and pharmaceutical drugs that can be purchased over- the- counter.

The Food & Drug Administration became a possibility because of the Pure Food and Drugs Act of 1906. Harvey Washington Wiley was the driving force behind this law and headed its enforcement, which provided basic elements of protection that consumers had never had before (FDA's Origin). The FDA is an agency that works within the US Department of Health and Human Services of the executive branch of government (About FDA). The Food and Drug Administration is responsible for protecting the public health of all Americans by ensuring the safety, efficacy, and security of a large range of products from drugs to cosmetics (What We Do).

The FDA also looks at several products that have chemical implications to them, such as drugs. It looks at drug manufacturing standards, as well as the labels of each drug (both over-the-counter and prescription drugs) and must give its approval on new drugs before they can be sold to the public. The FDA also looks at cosmetics. It must ensure that, like food articles, each product is properly labeled as to what comprises each item. Biological products, such as the nation’s blood supply, are also regulated by the FDA. It does research to improve upon the testing methods of blood, to ensure that the supply in hazard free. It also is in charge of handing out licenses to product and manufacturing establishments.

The U.S. Food and Drug Administration (FDA) is the governmental division that protects the public’s health by guaranteeing food, drugs, and medical devices are safe and effective. It assures that dietary supplements and cosmetics are well labeled, regulates tobacco, protects the users from electronic product radiation, among others.

“Pharmaceutical companies have a lot of money invested and push the FDA to approve their applications: “For example, since the 1938 legislation placed the burden of proof on the FDA when it came to challenging or delaying drug approvals, the agency's actions depended primarily on its budget. Larger budgets from politicians could engender greater scrutiny and more challenges of new drugs. Instead of reputation's facilitating such power, increased budgets and the pursuit of the agency's mission could also explain agency actions during 1944-61 “(FDA). “The Revitalization Act of 2007 further empowered the FDA. Legislation aimed at strengthening the US Food and Drug Politics are also played out in the media and indirectly influences whether an application is approved or removed such as

The FDA formulates rules, regulation and standards for allowing and certification of processed nourishment, drugs, food and other related products

Base on the sales representatives instructions, physicians started prescribing “opioids”. Shortly after, it was discovered that patient’s pain was relieved only for a small span of time, and when the pain came back it was more intense. Users had developed a resistance to “opioids”. Physicians then kept increasing their patient’s dose of medication, until the drug no longer had any effect on their bodies’ nervous system. Patients become accustomed to the fast release of endorphins cause by “opioids” (a chemical in the brain that naturally diminishes pain perception, and also acts like a sedative). Users began to notice the “rush” of the pain medication, like oxicodone (a fast relieve but short acting drug), oxicontine (extended relieve form of oxicodone) the most addicting form of “opioids”. By now they were not looking to ease their pain other that supply their dependency on the drugs. When Patients were no longer able to get enough medication from doctors, they either bought pills illegally or turned to a cheaper street drug, heroin, (a euphoric drug). “Heroin” affects the same brain receptors and provides the same “rush” effects like “oxicodone” enabling their

The Food and Drug Administration is the oldest consumer protection agency in United States (FDA 2). From recalls on food products to the monitoring of the safety of our medicine sources, the Food and Drug Administration (FDA) ensures that they are both safe and wholesome (FDA 1). The Food and Drug Administration also ensures that the cosmetics we use won’t harm consumers, and that radiation-emitting product such as microwaves are secure and effective (FDA 1).

The Food and Drug Administration was founded in 1906, through President Roosevelt. FDA is an agency part of the Department of Health. It was founded for the propose of protecting the public health, so that people were safe. FDA also helped to make sure that the production of cosmetics were under regulation and safe. Also it was used to help the consumers to get the best possible information they needed to help them safely choose their medicines and foods to help improve their health. Through the checking of meat, safety of medical devices, and nutrition information labeled on products, the FDA has helped people make sure the products people are using are safe to use and consume.

Painkillers are a great thing to have when the consumer is in pain, but when people abuse the pain killers this is when an issue is born. Depending on what the prescription is and the dosage could make it more dangerous. According to consumerreports.org, people who build up a tolerance to the painkillers can take higher doses without serious side effects. Also, often times the prescription is over prescribed and there are leftover pills after the consumer does not need to take them anymore. Unfortunately, with the abuse of prescription painkillers can indicate an addiction to heroin. There are many signs pointing to the consumers being at fault, but

The Federal Food, Drug Administration is responsible for establishing the Code of Federal Regulations which outlines the rules and regulations governing pharmaceuticals. The rules are divided into sections and include guidance based on drug categories. Due to each person having varying reactions to pharmaceutical products not all side-effects are detected during clinical testing. The Federal Food, Drug Administration is responsible for sharing the information with consumers. However, it seems a bit unethical because the large pharmaceutical companies do not have to share all of side-effect information that may assist consumers in making its choice on whether to try a product or to not try a product. Through various survey’s it was discovered that consumers are under the opinion that pharmaceutical companies need to have improved internal controls to ensure their compliance with regulations. Due to physicians and pharmaceutical companies working together and are dependent on one another there needs to be controls in place that would have an unbiased view of the regulations. The government will need to continue introducing new regulations that will aide in monitoring the relationships.

The FDA was created to oversee the quality of our food and medications to make sure they are effective and will not harm us.

The FDA is something that many people know about, but do not know what happens within the company. A majority of Americans have heard stories on the news of people making huge acquisitions of how the FDA killed their child by no correctly regulation fast food companies ; or how their husband died for a heart attack because the warning label on his bottle of medication was not correct.

The U.S Food and Drug Administration (USFDA) is the government agency responsible for ensuring the safety and efficacy of drugs and medical devices in the USA. The two legislative acts that are the main source of the FDA’s authority are: