A defective drug is any prescription or over-the-counter medication with serious or deadly side effects. Often times, a defective drug will make it into the market because the possible dangers were not identified or anticipated during clinical testing trials.
Each year in America, millions of people take prescription and over-the-counter medications to treat a variety of conditions, from minor colds to severe illnesses.
How a Defective Drug is Introduced into the Market
Pharmaceutical companies are driven by profits. This means that sometimes, in an attempt to increase sales, the safety risks associated with a certain drug will be overlooked. While it is the responsibility of the Food and Drug Administration (FDA) to determine whether a drug is safe for public use, the administration can also be at fault. If the FDA does not perform adequate research, or fails to administer the appropriate tests, a defective drug can be approved and introduced into the public sector.
The Drug Manufacturer’s Responsibility
A drug manufacturer must mandate all the necessary testing before seeking FDA approval for a particular drug. The manufacturer must also include any warnings about the side effects associated with that drug, along with possible complications of misuse. If an over-the-counter medication or prescription drug causes you serious injury, you can file a product liability claim to recover damages for your injuries.
A drug is deemed “defective” if the side effects associated with that drug outweigh its intended benefits. When this occurs, the FDA will issue a drug recall. Aside from drug recalls, the FDA will monitor drugs that are currently on the market and make changes to the labels, such as adding side effects and updating warnings as necessary. Consumer group petitions are also considered by the FDA.
Medications and Dangerous Side Effects
Side effects are the most common indicator that a drug may be defective. Several common side effects include:
- Liver damage
- Pulmonary dysfunction
- Increased risk of stroke or heart attack
- Kidney damage
- Heart damage
Dangerous Drugs to Watch Out For
Some of the more dangerous drugs include:
- Meridia: a prescription drug used to treat obesity related to high cholesterol and high blood pressure, Meridia can also cause stroke, rapid heart rate and seizures.
- Hydroxycut: this weight loss pill was recalled because its range of side effects, from insomnia to increased blood pressure to liver failure.
- Crestor: this cholesterol-lowering drug has been linked to kidney failure and rhabdomyolysis, a serious life-threatening muscle condition.
- Zicam cold remedies: these products were recalled because of their link to anosmia, the loss of sense of smell.
- Yaz Lawsuit: this birth control pill contains dropsirenone, which has been linked to serious medical conditions including blood clots, stroke, heart attack, gall bladder injury and deep vein thrombosis.
- Provigil: this medication is prescribed to promote wakefulness for those who suffer from sleep apnea and narcolepsy. The drug is under investigation for causing Stevens-Johnson Syndrome, a life-threatening condition that causes cell death in your skin.
- Accutane Lawsuit: this medication to treat acne can lead to birth defects, psychological side effects and suicide.
- Serevent: this asthma medication can increase your risk of an asthma-related emergency.
Article Source : The Cochran Firm – Defective Drugs : ArticleBase
Dangerous Drug Lawsuit Funding
If you have been injured by a defective drug or pharmaceutical, have retained an attorney, are currently in the process of waiting for your lawsuit to settle and are in dire need of immediate relief, give TriMark Legal Funding LLC a call. TLF is a leading provider of lawsuit funding and non-recourse lawsuit loans throughout the United States.
Please follow and like us: