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Millions of Americans rely on prescription medications to help manage your arthritis, heart disease, diabetes, psychiatric illness, hypertension, chronic pain, lung disease, and many other medical conditions. You have to trust the drug companies for safe, effective products to be developed. Too often, that trust is misplaced. Every year thousands of patients who are severely injured, and some were killed by the toxic effects of drugs and side effects are irreversible. This article can helpMore information about dangerous drugs.
Who is most at risk of dangerous drugs?
The elderly have a higher risk of dangerous drugs than the general population, since a large percentage of elderly take various drugs. The average senior takes five fifty-six prescribed medication, in addition to over-the-counter drugs. People aged 65 and over, however, only 14% of the U.S. population, but it takes more than 33% of all prescription drugs. This increased consumption isSeniors, many different drugs, and also increases the risk of dangerous interactions with other drugs.
If FDA approval means that a drug is safe?
FDA approval means that the U. S. Food and Drug Administration scientists have determined that the benefits of risk when the drug is released in the general population prevail. During the last phase of clinical trials before approval, as many of 3,000 people taking the drug. But some serious side effects are rare. If aSide effect occurred in one of 10,000 people, for example, the manufacturer and the FDA is unable to learn the side effects until the drug was approved, and hundreds of thousands of people took .
What is an adverse event?
The FDA defines an adverse event as adverse events associated with use of a drug to a patient. "
How does the FDA about side effects?
Doctors and health workers in general reportAdverse reactions to pharmaceutical companies, which are then legally required to report serious relay to the FDA within 15 days. Health professionals have to communicate if it leads to death, disability, hospitalization, life-threatening, causes a congenital anomaly or requires treatment to prevent permanent damage. Approved for the first three years after a drug, the drug manufacturer must also all its quarterly side effects to the FDA, and after three years, these reportsmust be provided annually.
How do I know if a drug is dangerous?
The FDA issued a notice of adverse events on their website, and these are frequently reported on the Internet, in newspapers and television news. drug manufacturers often warns health workers when they learn of adverse events associated with their products.
How do I know if my symptoms are the result of a dangerous drug?
For questions aboutThe symptoms and side effects, and any other aspect of your health you should consult your doctor. Your doctor can determine if a drug has led or contributed to your symptoms.
When I was injured or a loved one has been injured or died of drugs, what can I do?
You should, as soon as possible to talk with an experienced attorney to determine whether drugs may have a lawsuit against the manufacturer of the drug.
How important dopromptly?
Acting in a position soon to not make the difference between a case and a case. There are no time limits specified limitation period, with laws that establish rules for lodging complaints, which vary from state to state. . If you or a loved one has a serious injury or a loved one has died suffered a dangerous drug, you should not delay to contact an attorney. If the limitation period has expired, your right to exercise a right can neverbarred.
How difficult it is to manufacturer to win a claim against a drug?
Pharmaceutical companies are often large multinational companies with the staff of legal personality and substantial financial resources to defend their products. The upper hand against an opponent determined and well financed, you need an experienced pharmaceutical lawyer on your side, and a law firm that is committed to securing justice for their clients.
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