what are the side efects of drugs in a person
Answers
Answer:
1.Drugs ruined the life of man who takes Drugs.
2. It make drastic changes in the body of the person.
3. It makes the person addict.
Explanation:
Perhaps the most common set of side effects for drugs that work inside your body involves the gastrointestinal system. Nearly any drug can cause nausea or an upset stomach, though it may only happen to a handful of people. For drugs used on the outside, skin irritation is a common complaint.
An allergic reaction could happen with any drug. That can range from itching and rash all the way to a life-threatening anaphylactic reaction.
Some drugs can’t help but trigger side effects because of their chemical structure. The common allergy drug diphenhydramine (also known by the brand name Benadryl) is one. Though it eases allergy symptoms, it also blocks the chemical acetylcholine, and that leads to drowsiness and a host of other side effects, including dry mouth.
Some drugs have barely noticeable side effects at the right dose. Typically, warfarin (Coumadin, Jantoven), used to prevent blood clots, usually works well and isn't bothersome, but serious internal bleeding can happen in the wrong situation.
Side effects may show up only when a drug is mixed with certain other things. This might be called a drug interaction. For example, drinking alcohol while you're taking narcotic painkillers can cause an accidental overdose. This has led to many deaths. Another example is grapefruit juice, which can affect the blood levels of several drugs, including some blood pressure and cholesterol medicines.
Triple-Negative Breast Cancer (TNBC)
Triple-negative breast cancer is a rare type of breast cancer in which all receptor tests come back negative. It’s serious, but it responds well to treatment if you catch it early.
Still, sometimes testing doesn't reveal everything about a drug’s side effects, and they don't show up until after the medication enters the marketplace and more people start using it. That’s where MedWatch comes in. The FDA’s post-marketing surveillance program seeks voluntary input, mainly from health care professionals, on unwanted effects they see in ''the real world.'' Sometimes these reports are numerous or serious enough for the FDA to take regulatory action, such as adding warnings to a drug’s label.