Unapproved prescription drugs, unlike over-the-counter drugs, pose significant dangers to patients because the FDA has no not measured health, effectiveness or consistency. There is no way to know whether these medicines are safe and effective for their intended use, whether they are manufactured in a way that ensures good product safety, or whether they are packaged completely and correctly, without careful FDA review. Unapproved drugs have caused harm to patients and the Department aims to protect patients from the threats posed by these drugs. Many prescription medications exist on the open market, and millions of Americans attempt to avoid the process of obtaining a prescription from a doctor or certified pharmacist, going so far as to bribe pharmacists to obtain these medications. There are many prescription medications that are very popular in the United States. Some of these medications include atorvastatin, a medication often used to control high cholesterol levels in the human body. We also have levothyroxine, which happens to be an artificial thyroid hormone that helps people with thyroid deficiency, and omeprazole, which is a proton pump inhibitor prescribed to patients with digestive diseases such as ulcers. , acid reflux and gastroesophageal reflux also known as GERD. Say no to plagiarism. Get a tailor-made essay on “Why Violent Video Games Should Not Be Banned”? Get the original essay Prescription drugs are becoming easily accessible because the laws that should prohibit them are not strict enough. It's even difficult to tell the difference between prescription medications and over-the-counter medications because they seem to have a similar appearance. Experts in the medical field who have written and spoken in the past about unapproved drugs say prescription drugs existed until 1962, when the FDA's criteria for approval changed. The FDA sometimes allows pharmaceutical companies to promote imitations of their already approved drugs, as the companies provide information confirming the safety and effectiveness of their drugs. But most drug companies don't follow FDA guidelines, and the agency doesn't blacklist failing companies because they are overwhelmed by other significant problems. But the FDA has recently been cracking down on manufacturers of unapproved drugs by ensuring that they comply with FDA guidelines or risk having their drugs rejected from the market. Some of the unapproved medications on the market, such as the flu drug carbinoxamine, quinine, recommended for people with leg pain, and ergotamine tartrate prescribed for migraine, have all been linked to more than 'a hundred deaths. However, removing these drugs from the market is not as easy as one might think, some of these prescription drugs are very important and can be administered without the need for a prescription in emergency situations. If a pharmaceutical company submitted their drugs to the FDA for approval, they could obtain many economic benefits. The FDA, responsible for regulating the drug market, is responsible for ensuring that clinical drugs are researched and tested on humans to ensure their safety and effectiveness. Consumers of these drugs are cured, while drug manufacturers can.