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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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Jury Awards More than $2 Million in Actos Bladder Cancer Case

Oct 7, 2014
A jury in a Pennsylvania state court awarded more than $2 million to a woman who claimed Takeda Pharmaceuticals’ diabetes medication Actos...

Pennsylvania Jury Orders Takeda to Pay $2 Million in Actos Case

Oct 6, 2014
A jury has ordered Takeda Pharmaceuticals to pay more than $2 million to a woman who claimed the company’s diabetes drug Actos (pioglitazone)...

Doctors Receive Billions from Drug Companies

Oct 3, 2014
Drug and medical device companies pay billions to doctors, according to an online database compiled by The Centers for Medicare and Medicaid...

Hospira Receives FDA Warning Letter for Drug Manufacturing Violations

Oct 2, 2014
On Wednesday, Hospira Inc. said it had received a warning letter from the Food and Drug Administration (FDA) after an inspection of its Australian...

Eli Lilly Faces Lawsuit Over Testosterone Drug Axiron

Oct 2, 2014
In a recently filed lawsuit, Eli Lilly is accused of deceptively marketing the testosterone replacement drug Axiron while failing to warn about the...

FDA Updates Xolair Warning Label to Include Cardiovascular

Sep 29, 2014
There is a slight increased risk of cardiovascular problems associated with the asthma drug Xolair (omalizumab), the U.S. Food and Drug...

Male 'Enhancement' Drugs are Dangerous, FDA Warns

Sep 29, 2014
So-called “male enhancement” drugs are deceptive and can actually be life-threatening, according to the U.S. Food and Drug Administration...

Study Shows Increased Risk of Venous Thromboembolism in NSAID Users

Sep 29, 2014
A study published online last week in the journal Rheumatology shows a statistically significant increased risk of venous thromboembolism (VTE)...

FDA Warns Doctors of Fake Drugs

Sep 25, 2014
The Food and Drug Administration (FDA) issued a warning to doctors that the growing number of “rogue” wholesale distributors selling fake...

Pfizer Documents over Chantix should be Unsealed, Experts Say

Sep 18, 2014
Pfizer’s internal documents regarding the antismoking drug Chantix should be unsealed before the U.S. Food and Drug Administration (FDA)...

FDA Warns of Hypersensitivity Reactions with Over-the-Counter Acne Products

Sep 15, 2014
The Food and Drug Administration (FDA) has warned that over-the-counter (OTC) topical acne products containing benzoyl peroxide and salicylic acid...

Study Links Use of Viagra to Increased Risk of Melanoma

Sep 12, 2014
According to a study published online April 7 in JAMA Internal Medicine, men who use Viagra (sildenafil) may have a higher risk of melanoma....
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