Nonsteroidal Anti-Inflammatory Drugs Biology Essay Overview
Abstract. Nonsteroidal anti-inflammatory drugs NSAIDs, which work by inhibiting the cyclooxygenase COX isozymes, were discovered several years ago. They remain an important part of the pharmacological treatment of acute and chronic pain. The COX-COX- have different biological functions. Since the discovery of aspirin, small molecule drugs have been widely prescribed to treat inflammation and pain. Aspirin and several small molecule NSAIDs are known to inhibit nonsteroidal anti-inflammatory drugs. NSAIDs are one of the most commonly prescribed drugs to treat pain or fever. However, oral administration of NSAIDs is often associated with adverse effects due to their inhibitory effect on the constitutively expressed cyclooxygenase, COX-1, in, for example, the gastrointestinal tract. A systemic, nonsteroidal anti-inflammatory drug, NSAIDs have been recognized as a potentially serious threat to the natural environment. NSAIDs are popular painkillers, and the main way they enter natural waters is through discharges from wastewater and sewage treatment plants. To monitor infection caused by these medications, NSAIDs are nonsteroidal anti-inflammatory drugs that reduce inflammation, pain, and fever. There are many different types of NSAIDs, including nonprescription and prescription strength. Healthcare providers use them to treat a wide range of symptoms, from headaches and toothache to arthritis and muscle stiffness. Resume. INTRODUCTION. Nonsteroidal anti-inflammatory drugs NSAIDs, also called “aspirin-like drugs,” are among the most commonly used drugs. Aspirin itself was introduced by Bayer as a replacement for salicylic acid, which had been available in synthetic form for many years, and as the active ingredient. , pain and control of inflammation. However, an overdose of it can have harmful effects on the human body, while uncontrollable disposal in ecosystems poses significant environmental problems..