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Defective Drugs
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Just Because a Doctor Prescribes a Drug Doesn’t Mean It’s not Dangerous or Defective

Just Because a Doctor Prescribes a Drug Doesn't Mean It's not Dangerous or Defective

Just Because a Doctor Prescribes a Drug Doesn't Mean It's not Dangerous or Defective

Today, the pharmaceutical industry is producing drugs aimed at just about every ailment known to man, adding years to nearly everyone’s life, if not outright saving them. They also enable us to live a better-quality lifestyle for a much longer period of time.

Regrettably, some of the drugs these companies manufacture can ultimately prove to be defective, as well as dangerous – and even deadly. Sometimes it may take years for the side effects to even emerge – which means that ultimately some drugs on the market may end up doing more harm than good.

Like any other for-profit corporate entity, pharmaceutical companies are motivated, in varying degrees, by profit. Sometimes profits are more important than people. Anyone who reads the newspaper knows this to be a fact. In many a lawsuit, a pharmaceutical company will be charged with having known full well about some harmful side effect tied to its flagship billion-dollar powerhouse drug – in some instances, many years in advance of this fact’s public disclosure. Companies hide clinical evidence that a drug may be defective in order to gain the U.S. Food and Drug Administration (FDA)’s approval, and to not create obstacles to sales.

Prescription drugs with deadly or dangerous side effects are sometimes rushed to market without adequate testing, and often people are injured or die before the FDA can identify these drugs as having dangerous side effects that can far outweigh whatever benefits the marketing group had touted.

When an FDA classification leads to a drug recall and when an injury occurs, a lawsuit is frequently filed; drug recall lawsuits typically fall into a range of categories, including drug injury, product liability or medical malpractice lawsuits against drug companies.

If you or a loved one have been injured as a result of a prescription drug, you may have valuable legal rights. Parker Waichman LLP urges you to contact us by completing the form at right or call us at 1-800-YOURLAWYER (1-800-968-7529).

To view more information involving a specific defective drug, drug recall, or drug lawsuit, please click on one of the links listed below.

If the defective drug you are looking for is not below, please visit our Defective Drugs Archives page for additional articles about defective drug lawsuits that Parker Waichman LLP has defended for our clients.

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Defective Drugs

Defective Drugs NewsRSS Feed

Another Study Links Viagra to Increased Risk of Melanoma

Jul 21, 2015
The Journal of the American Medical Association (JAMA) has published study looking at the link between phosphodiesterase type 5 (PDE5) inhibitors,...

Combined Use of Antidepressants and NSAIDs Associated with Increased Risk of Bleeding

Jul 20, 2015
According to a new study, the combined use of antidepressants and a common painkiller is associated with an increased risk of intracranial...

FDA Warns of Heart and Stroke Dangers of Common Pain Relievers

Jul 17, 2015
The Food and Drug Administration (FDA) has warned that common painkillers like Motrin, Aleve, and Advil can increase the risk of a heart attack or...

FDA Talks with Google to See if Search Query can Help Identify Drug Side Effects

Jul 17, 2015
Discussions are in the works to determine how google searches may help the U.S. Food and Drug Administration (FDA) pinpoint drug side effects that...

CT Procedure Helps Identify Cause of Unexplained Pain after MoM Hip Replacement

Jul 16, 2015
A recently published study demonstrated that single photon emission tomography/CT (SPECT-CT) can be useful in identifying the cause of pain in...

New Study Suggests Increased Risk of Birth Defects with Prozac, Paxil

Jul 14, 2015
A new study published in the British Medical Journal (BMJ) adds to a body of research suggesting that the use of some antidepressants may be...

FDA: NSAIDs Increase Risk of Stroke, Warnings Strengthened

Jul 13, 2015
The warning label on non-aspirin, nonsteroidal, anti-inflammatory drugs (NSAIDs) is being revised to reflect an increased risk of heart attack or...

World Health Organization Issues Warning to India's Quest Life Sciences Over Drug Trials

Jul 13, 2015
The Indian clinical research organization, Quest Life Sciences of Chennai, has received a warning from the World Health Organization (WHO) over...

FDA Concern over Clot Risk for Eli Lilly Lung Cancer Drug

Jul 9, 2015
The Food and Drug Administration (FDA) is concerned that Eli Lilly & Co.'s experimental lung cancer drug may increase patients' risk of suffering...

FDA Announces Enforcement Action Against Unapproved Prescription Ear Drops

Jul 7, 2015
The Food and Drug Administration (FDA) has announced enforcement action against companies that distribute certain unapproved prescription ear drop...

FDA Investigates Serious Side Effects with Codeine Cough-and-Cold Medicine in Kids

Jul 6, 2015
The U.S. Food and Drug Administration (FDA) is looking into the safety of children's cough-and-cold medicines that contain codeine. According to a...

FDA Extends Deadline for Pharmacies' Track and Trace Compliance

Jul 1, 2015
The deadline for pharmacies to comply with federal track and trace requirements under the Drug Supply Chain Security Act (DSCSA) has been extended by...
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