Dr Shezad Malik Law Firm has offices based in Fort Worth and Dallas and represents people who have suffered catastrophic and serious personal injuries including wrongful death, caused by the negligence or recklessness of others. We specialize in Personal Injury trial litigation and focus our energy and efforts on those we represent.

Articles Posted in Toxic Injury

A Florida mother sued Fort Lauderdale Hospital and a psychiatrist who worked there, saying they overmedicated her teenage son with a cocktail of mental health drugs — some of which have not been approved for the treatment of children.

The boy, Emilio Villamar, died of a sudden heart attack. He was 16.

Emilio, a swimmer and water polo player, was diagnosed with bipolar disorder by Dr. Sohail Punjwani in March 2002. Within the next year, the teen was given 16 different psychiatric drugs, six of which were still being administered when he died, said Michael S. Freedland, who is representing Emilio’s mother, Norma L. Tringali.

Punjwani had also been treating 7-year-old Gabriel Myers, a foster child who had been prescribed several psychiatric drugs before he hanged himself in April. In the wake of Gabriel’s death, the Department of Children & Families has launched a wide-ranging investigation into the agency’s dispensing of mental health drugs.

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Asbestos is a naturally occurring fiber that, when released into the air, can be inhaled or swallowed. Asbestos fibers are so small that they are not visible to the naked eye. Once they are inhaled, asbestos fibers stay in the body and, over the course of decades, lead to the development of asbestos-related diseases like mesothelioma.

Mesothelioma is rare form of cancer caused by asbestos exposure. An estimated 3,000 Americans are diagnosed with mesothelioma each year, and because the disease takes decades to develop, the rate of new diagnoses is still climbing. The peak incidence of mesothelioma is predicted to occur around 2020.

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Nearly three of 10 teenage Florida foster children have been prescribed a mental-health drug, and 73 foster kids younger than 6 are taking mind-altering drugs, according to a recent study released in response to the death of a Broward foster child who was taking such medications.

In all, 2,669 children — or 13 percent of Florida foster children — are being given powerful psychiatric drugs, said the study, commissioned last month by Department of Children & Families Secretary George Sheldon. The largest group, almost 60 percent, are teens ages 13 to 17.

The 2,669 children represent about one-third more kids than a DCF database had reported as taking mental-health drugs — meaning electronic state records had significantly underestimated the use of mind-altering drugs.

Child-welfare administrators are investigating the use of mental-health drugs by children in state care in the wake of the April 16 death of Gabriel Myers, a troubled 7-year-old boy who hanged himself in the shower of his Margate foster home.

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Two class action lawsuits have been filed in the wake of the recall of Hydroxycut, a popular weight-loss supplement that has been linked to liver damage and other life-threatening side effects.

The suits, filed in Canada and Tennessee, accuse Iovate Health Sciences, which manufactures Hydroxycut, of failing to warn of the drug’s dangers or take proper precautions to protect its users.

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GlaxoSmithKline, maker of Avandia, faces more lawsuits alleging that patients suffered from serious Avandia side effects. Among the more severe side effects is the reported link between Avandia and heart attacks. Some critics say the risk of a heart problem is too high, while patients file lawsuits alleging they were harmed by the use of Avandia.

One such lawsuit was filed in Texas, alleging the plaintiff, Frank Casteel, took Avandia for 5 years and then underwent heart bypass surgery. According to the Southeast Texas Record, the suit was filed against Smithkline Beecham Corp., doing business as GlaxoSmithKline. The plaintiff claims that GlaxoSmithKline knew its drug was unreasonably dangerous, knew that patients were not informed about the risks associated with Avandia and still marketed and distributed the drug. Furthermore, the suit alleges that the pharmaceutical maker disclosed positive information about Avandia, but concealed or withheld any negative information about the drug’s safety.

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Federal drug regulators warned consumers to stop using the popular Hydroxycut line of weight-loss products, citing reports of a death due to liver failure and other instances of serious health problems.

In all, the Food and Drug Administration said it had received 23 reports of significant adverse health effects in people who used Hydroxycut, including one person who required a liver transplant. Other complications included heart problems and a kind of muscle damage that could lead to kidney failure, the agency said.

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After three days of deliberation, a McLean County jury awarded the family of a deceased Bloomington woman more than $2 million related to her exposure to asbestos.

Juanita Rodarmel contracted mesothelioma after being exposed to asbestos when she laundered the clothing of her first husband, Leslie Corry, a worker at the former Union Asbestos & Rubber Company.

Corry worked at the Bloomington plant, later called UNARCO Industries Inc., during the 1950s.

The jury also awarded $100,000 in punitive damages against Pneumo Abex, LLC and $400,000 against Honeywell International, Inc.

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A Maricopa County Superior Court jury has awarded $3.3 M to a Scottsdale woman who was sickened and permanently disabled by a mold infestation in her apartment building.

Robin Minium was a project manager for American Express and worked out of her upscale apartment near Scottsdale and Bell roads. She had lived there since 2000.

According to court documents, her health deteriorated significantly by 2002, and as she got sicker, she spent more time in her apartment.

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Just two months after the U.S. Supreme Court decided patients can sue drugmakers over injuries from medicines approved by the government, long-stalled lawsuits against GlaxoSmithKline Plc and Bristol-Myers Squibb Co. are again moving toward trials.

The March 4 decision in a case on Wyeth’s nausea treatment Phenergan broke a logjam of cases in state and federal courts. Federal regulatory approval of a medicine and information about side effects does not shield drugmakers from claims that patients and doctors were not adequately warned, the high court ruled. The decision already affected more than 250 lawsuits involving at least 10 companies that were in limbo before the ruling.

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The U.S. Supreme Court cleared the way for a suit by a New Jersey woman who claims to have suffered mercury poisoning from Chicken of the Sea canned tuna.

The denial of certiorari sets the stage for a federal court trial in Newark, N.J., in a putative class action suit, filed under New Jersey’s Product Liability Act, that faults a cannery company with not putting mercury warnings on the label.

The justices without opinion let stand a 3rd U.S. Circuit Court of Appeals ruling last September that the claim is not pre-empted by the Food and Drug Administration’s “pervasive regulatory scheme.” The appeals court said this is a case where state tort law complements federal regulations, which often lack a compensatory apparatus or a process for gathering information about potential claims.

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