Unapproved prescription drugs, unlike over-the-counter drugs, pose significant dangers to patients because the FDA has not measured the health, effectiveness or coherence. There is no way to tell whether such drugs are safe and effective for their intended use, whether they are manufactured in a way that ensures good product safety, or whether their packaging is complete and correct, without FDA scrutiny. Unapproved drugs have caused harm to patients, and the Department aims to protect patients from the threats raised by such drugs. Many prescription drugs exist on the open market as millions of Americans trying to get through the process of getting an actual prescription from a certified doctor or pharmacist go so far as to bribe pharmacists to obtain those drugs. There are many prescription drugs that are very popular in the United States. Some of these drugs include Atorvastatin, which is a drug often used to control high cholesterol levels in the human body, we also have Levothyroxine, which is an artificial thyroid hormone that helps people suffering from thyroid deficiency, and l 'Omeprazole, which is a proton pump inhibitor prescribed to patients suffering from digestive diseases such as ulcers, acid reflux and gastroesophageal reflux disease also known as GERD. Say no to plagiarism. Get a tailor-made essay on "Why Violent Video Games Shouldn't Be Banned"? Get an Original Essay Prescription drugs are becoming easily accessible because the laws that should outlaw them are not robust enough. It is even difficult to distinguish between prescription drugs and over-the-counter drugs because they appear to have similar appearances. Medical experts who have written and spoken about unapproved drugs in the past assume that prescription drugs existed until 1962, when the FDA's criteria for drug approval changed. The FDA sometimes allows drug companies to promote imitations of their already approved drugs, as the companies provide information supporting the safety and effectiveness of their drugs. But most drug companies fail to follow FDA guidance, and the agency doesn't blacklist non-compliant companies because they are overwhelmed by other important issues. But in recent times the FDA has been cracking down on manufacturers of unapproved drugs by ensuring that they comply with FDA directives or risk seeing their drugs kicked off the market. Some of the unapproved drugs on the market such as carbinoxamine, an anti-flu drug, quinine, recommended for people suffering from leg pain, and ergotamine tartrate prescribed for migraines, have all been linked to over a hundred deaths . However, taking these drugs off the market is not as easy as you might think, some of these prescription drugs are very important and can be administered without a prescription in emergency situations. If a pharmaceutical company were to submit their drugs to the FDA for approval, they can gain many economic benefits. The FDA, responsible for regulating the drug market, is responsible for ensuring that clinical drugs are researched and tested in humans for safety and effectiveness. Consumers of these drugs recover, while drug manufacturers can obtain essential tax subsidies for some drugs. The FDA offers orphan drugs a special status that allows drugmakers to create therapies for uncommon diseases. These benefits may result in faster times for acceptance and financial aid. Furthermore, manufacturers can