1906 Drug Administration

In 1906 the Food and Drug Act was officially created by the president at the time that was Theodore Roosevelt. The job of the FDA is to protect the health of the public and doing so by assuring that human and veterinary drugs are safe and secure along with biological products, medical devices , food supply in the US, cosmetics, and products that have been introduced to radiation. It’s important because they ensure the foods you are consuming can be eaten without getting you sick. They also ensure the medicine you get is not going to cause harm to you. Without the FDA the drugs we get from pharmacies and the food we get from stores would have the possibility of being very unsafe and hurtful. The FDA has created many regulations that products have to go through to be considered FDA approved. Some of those include the safety of the food we consume, products that contain tobacco, dietary supplements, medications from pharmacies, vaccines, and blood

The US Food and Drug Administration is a branch of the US Department of Health and Human Services. The Office of the Secretary, HHS’s chief policy officer and general manager, administers and oversees the organization, its programs, and its activities. The Deputy Secretary and a number of Assistant Secretaries and Offices support OS. (Message from HHS) The FDA is

FDA's organization consists of the Office of the Commisioners and four directorates overseeing the core functions of the agency: Medical Products

As one of the primary federal consumer-protection laws in existence today, The Federal Food and Drug Act of 1906 was a law that had two primary goals for food and drugs: (a) forbid harmful ingredients and additions and (b) demand labeling of ingredients to inform consumers. According to Janssen (1981), it was hoped that the enactment of this law would eliminate adulterations and poisons sometimes found in foods, sometimes in drugs and often in both. The foundation of food and drug protection came from the development of scientific methods of analysis by the Federal Bureau of Chemistry,

The first Pure Food and Drug Act was put into action by Theodore Roosevelt in 1906. The act was passed to prevent the manufacture, sale, or transportation of misbranded or harmful food, drugs, medicines, and liquors. Due to this act the Food and Drug Administration (FDA) came to be. The FDA is now responsible for the testing of all foods and drugs for human consumption and the label warnings on them as well.

The FDA received it start under a different name. First called the Division of Chemistry, which played a small part in everyday life, then in July of 1901, the name was again changed to the Bureau of Chemistry. The FDA that we now know came from the passage of a bill in 1906, the Federal Food and Drug Act shaped the role that the FDA would come to play. The bill gave the FDA its power to regulate over a wide subject matter.

Bibliography Medicine and Health in the 1930s: Overview. (np) History Gale. 2003. Web.

Methaqualone, is also referred to as Disco Biscuits, Down And Dirties, Jekyll-and-Hyde, Joe Fridays, Lemmon 714, Lemons, Lennon's, Lovers, Ludes, Mandies, Mandrake, Q, Qua, Quack, Quad, Quaaludes, Soaper, Supper, Vitamin Q, The Love Drug, Wallbangers, Whore Pills, and Sopor. This list of street names for the drug goes on and on.

Narcotics are central nervous system depressants that relieve pain without causing the user to lose consciousness. It is this reason many people choose to abuse prescription narcotics.

The Food and Drug Administration was founded on June 30, 1906 by then US president Theodore Roosevelt and Harvey Washington Wiley. It was formed as a response to serious abuses that were taking place at the time. In the government structure the FDA is a federal independent executive agency so that means that it is like a cabinet but it doesn't have the statues that some other agencies would have. And now I will go over why the FDA is necessary and what they do in it.

The intended use of medications is meant to improve a person’ health, it is very important the individual administering medication or self-medicating use the drugs correctly, by following the doctors’ instruction for the medication prescribed. Medication is given to diagnose, treat, and prevent illness. Medication can be very dangerous, which can potentially cause harm or even deaf if it’s not used properly.

It also regulates various other products, including food, cosmetics, veterinary drugs, radiation-emitting products, biological products as well as tobacco products. The FDA is one of the United States federal executive departments and is also a federal agency of the United States Department of Health and Human Services. The APA is simply a federal law that governs the way the FDA and other administrative agencies propose, constitute, and establish

The FDA is and agency that falls into the Department of Health and Human Services under the Executive Branch, probably the most interesting agency in my eyes because of its importance in the nation and how a mistake from them or maybe a wrong move can be lethal. This very important agency can actually be traced back to the 1800's but bills were placed after it earlier agencies to become what it is today after protests and cries of those living in the nation around the early 1900's. (Office of the Commissioner) Its food we are talking about and food is something we insert into our body including the drugs we take. Therefore, it involves with our daily lives and with them being around it can protect us form the threats of health out there.

"Education never ends, Watson. It is a series of lessons, with the greatest for the last."

Correct (chemical & name brand) Name of drug. What category of drug is it? What schedule