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DEFECTIVE DRUGS

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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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...

Harvard Doctor Warns Against Loosening Restrictions for Off-Label Marketing

Jul 1, 2015
The U.S. Food and Drug Administration (FDA) is holding a meeting to discuss its restrictions on off-label marketing, which is when drug companies...

Advocacy Groups File Lawsuit against FDA over Gilead Hepatitis C Trial Data

Jun 30, 2015
Two consumer advocacy groups are suing the U.S. Food and Drug Administration (FDA) over clinical trial data for Gilead Sciences hepatitis C drugs....

Some Sleeping Pills Increase Risk of Respiratory Cancers

Jun 24, 2015
New research shows that some of the most widely used sleeping pills taken worldwide could triple the risk of lung cancer. The new study warns that...

Viagra Use Could Increase Skin Cancer Risk by 20 Percent

Jun 24, 2015
Men who use Viagra and similar drugs for erectile dysfunction could be at greater risk of developing skin cancer, according to a new study. A study...

FDA Part of International Action Against Internet Sales of Unapproved Drugs and Medical Devices

Jun 19, 2015
In a news release issued on Thursday, the Food and Drug Administration (FDA) said it had sent warning letters and seized potentially dangerous,...

Proton Pump Inhibitors May Increase Heart Attack Risk

Jun 18, 2015
A recent study shows that people who take proton pump inhibitor drugs for gastroesophageal reflux disease (GERD) are at increased risk for heart...

FDA Mistakenly Expands Approval for Sleep Drug

Jun 15, 2015
When the Food and Drug Administration (FDA) gave approval for Hetlioz (tasimelteon), a drug to treat non-24 sleep-wake disorder, a rare condition,...

Drug Companies Hide Reasons Drugs are Rejected by FDA

Jun 15, 2015
On seven occasions between August 11, 2008, and June 27, 2013, the Food and Drug Administration (FDA) denied approval to a new medicine, in part,...

Lawmakers Urge FDA to Add Boxed Warning to Immediate-Release Opioids

Jun 11, 2015
Legislators are calling on the U.S. Food and Drug Administration (FDA) to add a boxed warning, or black box warning, to the label of...

Pain Pill Abuse May be Contributing to Indiana HIV Outbreak

Jun 11, 2015
The newest formulation of the prescription pain pill Opana could be contributing to an HIV outbreak in Indiana. In May 2013, Food and Drug...

Potential Link between Zoloft and Birth Defects Identified in Pfizer Report

Jun 10, 2015
A Pfizer report warning that Zoloft may be linked to birth defects may make it more difficult for the pharmaceutical company to dodge litigation,...
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