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 Wrongful Death

Byetta which is used to treat Type 2 diabetes, has side effects that could increase the risk of serious and potentially life threatening pancreatitis.

Reports have found an association between Byetta and pancreatitis. Amylin Pharmaceuticals and Eli Lilly & Co., the manufacturers of the defective drug have failed to adequately warn about the risk of the serious and potentially fatal injury.

Byetta lawsuits are being investigated for users diagnosed with:

* Acute Pancreatitis
* Hemorrhagic Pancreatitis
* Necrotizing Pancreatitis
Potential cases are being evaluated throughout the United States.

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A jury deliberated less than an hour before award­ing $3.5 million to the family of a man who died when his van was crushed between two logging trucks in a January 2008 acci­dent in Elmore County.

A Chilton County jury ordered Ken Gorum Trucking and Gary Fruge, the driver of the logging truck, to pay $3.5 million to the family of James Sanderson.

Attorneys Benjamin E. Baker and J. Cole Portis entered evi­dence that the Gorum truck was being operated at a high rate of speed and with defective brakes in violation of Alabama law.

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Yasmin lawsuits are personal injury cases that seek settlements for women injured after taking Yasmin (drospirenone), a contraceptive pill also prescribed in the treatment of moderate acne and premenstrual dysphoric disorder (PMDD) for menstruating women. Yasmin may also be sold under the brand name Yaz, a form of drospirenone manufactured and distributed by Bayer.

Produced by Berlex Laboratories, Inc., Yasmin has been reported to cause a variety of serious side effects since its FDA approval in May 2001. Women injured after taking Yasmin will likely be entitled to compensation by pursuing a Yasmin lawsuit.

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Patients who were harmed because of heparin contamination still have time to bring claims against the makers of the heparin products. Patients may have been exposed to contaminated heparin through injections, pre-filled syringes or IV bags. It is important for people affected by contaminated heparin to hold those responsible accountable for what happened.

Heparin is a blood thinner, used in a variety of procedures, including dialysis and cardiac procedures. In early 2008, the US Food and Drug Administration (FDA) announced a recall of certain Baxter heparin products after the agency received reports of adverse reactions linked to the products. Within a month, hundreds of reports detailing severe reactions to heparin surfaced worldwide. The recall was later expanded to include more products and other companies.

The FDA discovered that the contaminant was oversulfated chondroitin sulphate (OSCS), the reactions to OSCS can be extreme; with large doses of heparin, it can result in death.

Injuries linked to contaminated heparin include nausea, vomiting and flu-like symptoms to anaphylactic shock, coma and even death.

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Accutane has been a controversial acne medication because of the serious risk of side effects and suicides attributed to it. The FDA warned physicians prescribing the acne medication to be aware of any signs of depression their patients might display. Accutane manufacturer Hoffman-LaRoche did not warn patients and healthcare professionals of the potential risks involved with Accutane until after the FDA made this advisement.

In October 2001, Congressman Bart Stupak expressed his concerns about Accutane following the suicide of his son who was taking Accutane. Accutane manufacturer has warned physicians that the acne drug can possibly cause “depression, psychotic symptoms, and rarely suicide attempts,” but still the company maintains they believe the drug is safe. In addition, Accutane carries high risk of serious birth defects, including deformed babies, miscarriage, premature birth, or death of the baby.

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The parents of a toddler who died July 1 in a locked minivan outside a Bucks County daycare center – forgotten there for more than six hours – have filed a negligence lawsuit against the center and its owners.

Daniel Slutsky, 2, died of hyperthermia in the back seat of a van belonging to his neighbor, Rimma Shvartsman, a co-owner of Fairy Tales Daycare Center in Penndel.

In the suit, filed in Philadelphia, Gil and Lyudmila Slutsky seek an unspecified amount of damages, saying Fairy Tales and its owners “were under a legal and moral duty to provide competent and safe care” for their son.

Law enforcement authorities are still investigating the death, and Bucks Count District Attorney Michelle Henry has not ruled out possible criminal charges.

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If you are a patient taking Avandia and have suffered a heart attack or stroke, you need to seek legal advice as the time for filing a lawsuit may be running out, . Avandia is used to treat type 2 diabetes mellitus but studies have linked Avandia to an increased risk of adverse heart events.

Avandia was found to have an increased risk of heart attacks and strokes, the problems it causes are similar to those caused by Vioxx. Avandia is believed to increase a certain subset of cholesterol that also increases the risk of heart attacks.

The FDA issued a safety alert in May, 2007, based on different studies, and found that people with underlying heart disease are at an increased risk of one of those events [heart attack or stroke] if they are taking Avandia. There was a meta-analysis, where researchers looked at different studies, and that showed a 30 to 40 percent greater risk of a heart attack in patients treated with Avandia than people treated with a placebo or other diabetes therapies.

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Introduced in the U.S. in July 2002, NuvaRing is a vaginal contraceptive ring that is over 98 percent effective at preventing pregnancy when it is used properly.

NuvaRing birth control works over the course of three weeks by slowly releasing hormones into a woman’s body. While NuvaRing needs to be removed during the fourth week of a month (to allow for menstruation), the contraceptive effects of this birth control device continue to persist.

Currently, over 1.5 million women in 32 countries, including the U.S., the Netherlands and Australia, use NuvaRing.

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According to adverse drug event reports received by the FDA, there may be a connection between the use of Chantix and diabetes. The drug has been linked with a number of reports involving new onset diabetes.

The Chantix attorneys at Dr Shezad Malik Law Firm are evaluating the potential for legal cases on behalf of individuals who were diagnosed with diabetes for the first time after using Chantix.

While studies have not firmly established that Chantix causes diabetes, sufficient reports of problems associated with the use of the drug warrant further investigation. Potential cases are being reviewed throughout the United States.

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The use of oral sodium phosphate products, like Fleet Phospho-soda, Visicol and OsmoPrep, to clear out the bowels before a colonoscopy or other medical procedure, have been associated with the development of a rare but serious form of kidney injury known as acute phosphate nephropathy.

The Fleet Phospho-soda attorneys at Dr Shezad Malik Law Firm are investigating potential Acute Phosphate Nephropathy lawsuits for patients who have been diagnosed with the kidney condition after using an over-the-counter Fleet Phospho-soda laxative at high doses for colonoscopy prep.

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