Defective Drug, Dangerous Drug and Pharmaceutical Drug Litigation

Pharmaceutical drug litigation cases are governed by federal laws, and the outcome-based sustentative properties of such cases, including statutes of limitations and the product liability laws themselves, are governed by the state in which you live. 

Defective Drug News

The FDA announced on June 16, 2009 that they advise consumers not to use Zicam cold remedies due to their link to anosmia, the loss of sense of smell. The three Zicam products the are referring to are:

-Zicam Cold Remedy Nasal Gel
-Zicam Cold Remedy Nasal Swabs
-Zicam Cold Remedy Swabs, Kids Size*
*(a discontinued product)

If you would like to learn more about the Zicam side effects or would like to discuss your Zycam injury with a defective drug lawyer, Phillips and Associates can help you pursue a Zicam lawsuit. Simply fill out the form on the right side of the page or pick up the phone and call our attorneys today.

Read more about the Zicam Injury Warning

The entire line of Hydroxycut products have been officially recalled by the Food and Drug Administration (FDA) due to the serious side effects that have been reported after use of the products. The problems caused by Hydroxycut ranged in seriousness from relatively mild, such as lack of sleep, to more serious, including a rise in blood pressure, to most serious, which included liver failure and even one death.

If you would like to learn more about the Hydroxycut Recall or would like to discuss your Hydroxycut claim with a lawyer, Phillips and Associates can help you pursue a Hydroxycut lawsuit. Simply fill out the form on the right side of the page or pick up the phone and call our attorneys today.

Read more about Hydroxycut

Chantix was banned by the FAA for pilots and other avation personal on May 21, 2008. Now the drug has been banned for use in truckers and bus drivers.

The U.S. Food and Drug administration recently issued a public health advisory on Chantix after a series of CBS 11 reports on the drug's serious side effects, including violent behavior and suicidal thoughts.

Read more about Chantix

Trasylol was approved in 1993 but questions about its safety didn't surface until 2006, when one large study linked it to increased risk of death, heart attack, stroke and kidney failure. An analysis of the data showed Trasylol increased chances of death by 54 percent. Bayer has yet to remove the drug from the market.

Read more about Trasylol

Although the product had been approved for use by the FDA several years ago, recent events have shown that the NuvaRing could cause serious side effects. Long-term exposure to high levels of estrogen and progestin have also shown a tendency to lead to blood clots and pulmonary embolisms, which are blockages of the pulmonary artery. 

Read more about Nuvaring.

UPDATE: SEPTEMBER 10, 2007: Study on Drug Safety shows Deaths related to Consumer Drugs on the Rise.

A recent study published September 10, 2007 by the Institute for Safe Medication Practices, in Huntingdon Valley, Pa. has illustrated that the number of serious adverse drug events more than doubled between 1998 and 2005 in the United States.

Read more about deaths related to Consumer Drugs by clicking on the link.

Drug Injury Cases:

These cases are brought by injuries caused as the result of a product known to be potentially dangerous which was sold without a proper warning to the consumer. This includes prescription and over-the-counter drugs sold without a warning of the hazards of use with certain other drugs, excessive long-term consumption, possible side effects of use, or withdrawal symptoms that could occur when trying to reduce the dosage or quit the use of a drug altogether.

Defective Drug Class Action Lawsuit.

If you are a part of a large group of people that has been similarly injured by the same defective drug product, you may qualify to start or join a class-action lawsuit. The designer, manufacturer, and others involved in the chain of commerce, including the distribution of the products that caused the injury or illness, can be held liable for injuries and illnesses caused by the defective drug product. There are many benefits to joining a class-action lawsuit, and a qualified drug litigation lawyer can provide the necessary legal advice on whether it would be best to start or join a class-action or pursue your claim as an individual lawsuit--if it's been determined that you do in fact have a legal claim.

Defective Drug Injury Case.

A defective drug product is one that causes a physical injury or illness (including psychological and/or mental illness) to a person as the result of a defect in the medication or its labeling.

These products can include prescription pharmaceutical drugs and everyday over-the-counter medications. Sometimes it can take years to discover that a medication could be dangerous or otherwise defective, and this typically occurs after several people have already suffered debilitating injuries or wrongful death due to their use of such products.

If you or a loved one has been injured or has fallen ill due to what you believe is a defective drug product, do not delay in seeking immediate medical attention, as prompt diagnosis and treatment may help to avoid irreparable damage.  It is also important to take immediate legal action, as restrictive statutes of limitations can prevent you from collecting the compensation you are entitled.  Successful defective drug litigation sends a clear message to the pharmaceutical industry about accountability and consumer safety.  For more information, contact a skilled defective drug litigation attorney who is experienced in this area of law.

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