The term "recalled drugs" refers to any type of medication, whether it is prescription or over the counter, that has been withdrawn from the market, either by the particular drugs manufacturer or the FDA, also known as the Food and Drug Administration. The Food and Drug administration is a business entity that is responsible for making sure that foods, drugs and medical devices are safe for consumers. When it has been determined that a drug has such adverse side effects that injury or death could be a result of their use, the Food and Drug Administration will issue a recall. In addition to the two types of drug recalls that can be issued, which include Class I and Class II Recalls, the Food and Drug Administration also issues safety alerts, notices and warnings. They also have the ability to implement labeling changes for certain drugs that may pose an inherent risk.
Recalled drugs that fall under a Class I Recall carry the reasonable possibility that their use, or exposure to them may cause serious injury and maybe even death. Recalled drugs that fall under a Class II Recall have the potential to cause temporary or medically reversible injury.
Defective Drug Lawsuits:
In the recent past there have been many research studies conducted regarding recalled drugs, and it was found that since 1993, there have been over 1,000 deaths can be linked to pharmaceutical drugs. It is also a widely reported fact that over 20 million people have at one time taken a drug that was eventually recalled. Newspapers and television alike are constantly reporting on recalled drugs and the lawsuits that are filed because of them. Billions of dollars are awarded every year to patients, as well as their surviving family members, who have incurred serious loss or injury due to the adverse effects of recalled drugs.
Recalled drugs have been known to cause birth defects, heart attacks, strokes, deadly breathing problems, death, and many, many more potentially dangerous adverse affects. While drugs do undergo lengthy testing procedures and resting phases before being approved for public use, it sometimes is not apparent just what the effects will be until a large, diverse group of people have begun to use the drug. Sometimes, at this point it is too late, as they drug may have been responsible for someone's death.
The list of recalled drugs keeps growing as time goes by, and many consumers are beginning to wonder just how safe the drugs are that they take on a daily basis.
| Crystal says: | 2006-10-19 11:31:33 |
| great information on recalled drugs | |
| Levette says: | 2007-01-25 07:24:57 |
| My father pass away 2 years ago. He use several of these recall drugs (Baycol,Bextra,Vioxx). Can I still file in his behalf. | |
| Belinda says: | 2007-04-12 23:23:57 |
| I have taken VIOXX, BEXTRA, and CELEBREX over the past 3 years now I am having some blood pressure problems and palpitions could this be from these drugs? Can I file on this? | |
| cameron says: | 2008-03-06 13:07:18 |
| testing | |
| Laura says: | 2008-07-23 08:38:37 |
| I took an antibiotic drug called omnicef.After taking this drug i was diagnosed with a leaky heart valve.It put me in the hospital for a week.my liver enzymens went out of whack. do i have a case | |
On January 31, 2008 The FDA announced a recall to consumers and healthcare professionals that NuCel Labs has voluntarily recalled all Eye Drops and Eye/Wash Products. This is a nationwide recall due to testing which indicated potential bacteria and particulate matter making the products non-sterile. Use of the products poses an unacceptable risk of eye infections and in rare cases blindness or loss of vision.
Why are drugs recalled?
If a drug has been shown to produce adverse side effects in a disproportionate number of cases then the FDA and the manufacturer will recall the drug. When a drug is recalled it usually means production is stopped and unused portions of the recalled drug are returned. Sometimes the drugs are stopped permanently, sometimes they are returned to the market but their use limited.
How do defective drugs make it onto the market?
The drugs and Pharmaceutical companies are a multi billion dollar business in America. Many of these companies will go to less than scrupulous lengths to insure the profits keep rolling in. Some streamline their testing , Omit key facts as well as pressure FDA officials. The FDA as well has never had the best reputation for follow up studies. Sometimes it takes time for symptoms to show so without follow up studies damage can be done without people knowing it.
How do I find out which are the recalled drugs?
The internet is a fantastic source. The food and drug administration website will list all products recalled and their current status. Some other good sources are web MD. .Com and Medical malpractice attorney websites. They will tell you the most dangerous, the risks and what you should do if you have been prescribed a recalled drug.
What can I do if I have been prescribed a recalled drug?
You need to speak to your doctor about possible risks to your health. If you have suffered due to a recalled drug you may be entitled to monetary compensation. Your best advice is to contact a medical malpractice attorney who is well known in the facts. They will be able to advise you on the merits of your case and what your options are.
Companies are liable for their products so don't put up with needles suffering due to a recalled drug. Get advice as soon as possible.
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