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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.

SSRIs are a widely prescribed class of drugs most often used as antidepressants to treat depression and anxiety disorders. Since September 2005, scientific information has been emerging that certain SSRIs, such as Celexa (citalopram), Lexapro (escitalopram), Prozac (fluoxetine), and Zoloft (sertraline), and SNRI antidepressants, such as Effexor (venlafaxine) may cause birth defects.

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SSRI Birth Defects

Cardiac (heart)

This is an interesting issue of conflict of interest, impartiality and doing the right thing, as reported by the Wall Street Journal.

Talk about the fox guarding the chicken house! In December, an advisory panel for the U.S. Food & Drug Administration (FDA) voted to recommend by 15-11 margin that the benefits of Yaz, Yasmin and similar pills made with the synthetic progestin, drospirenone, outweighed their risk of dangerous blood clots.

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Now it has come to light that three of the FDA advisors who voted with the majority had ties to Bayer AG, the maker of the drugs, that were not disclosed by the agency.

I am providing this timely slip and fall update. Unfortunately many folks get injured by slipping and falling in a Dallas store or businesses every day. Many serious injuries can be avoided if Texas’ business owners would simply take the time and invest the money to make their stores safer.

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As a Texas supermarket trip and fall attorney, I have represented customers who have been injured in grocery stores, convenience stores, shopping malls and big-box retailers for many years. Consistently, I have found that most of our clients have fallen because the business owner has not dedicated enough resources to customer safety. Some companies spend millions advertising each year but skimp when it comes to keeping customers safe.

Customer safety begins by creating the safest environment reasonably possible. Stores should have adequate lighting, clean and clear places to walk and non-slip surfaces. Many people in the Dallas Fort Worth area walk around in sandals and open-toed shoes. Knowing this, extra precautions should be used by store owners to make sure that anti-slip surfaces and anti-slip wax are used.

I am providing this important update regarding car safety and car accidents. Since our Fort Worth car accident lawyers have represented injury victims for many years we understand that while some accidents are unavoidable the extent of the injuries often depends on the safety of the cars involved.

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Very often, the difference between a safe car and one that fails to meet national standards can mean the difference between simply walking away from an accident or being seriously injured or killed.

The Insurance Institute for Highway Safety (IIHS) is a not-for-profit group financed entirely by the insurance industry. As a Tarrant traffic accident lawyer, we study closely the recently released IIHS 2012 list of Top Safety Picks, with a record breaking 115 passenger vehicles receiving the distinction of being a Top Safety Pick. Utilizing the IIHS study will help drivers make better-informed selections about the cars they drive.

Analysis of data from the Women’s Health Initiative, postmenopausal women who were on a statin at study entry had almost a 50% greater risk of diabetes than those who weren’t on the cholesterol-lowering drugs, according to a report in the Archives of Internal Medicine.

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Following the lead of the Federal Court ordered mediation in the Yaz/Yasmin litigation, the Pennsylvania state court judge has entered a similar order.

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Judge Moss, who is managing thousands of cases in Philadelphia state court, required mediation in an order published on January 6, 2012. Judge Moss’s order comes just one week after a federal judge entered a similar order.

Both judges appointed Professor Stephen Saltzburg of George Washington School of Law, Washington D.C., to assist in the mediation.

Novartis is under the gun over the deadly side effects caused by Tekturna (Aliskiren), its blood pressure pill, the so called “wonder drug.”

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Recently Tekturna’s clinical trials were canceled by Novartis due to a high number of strokes and kidney problems among diabetic test subjects. Tekturna HCT, Valturna, TekAmlo and Amturnide are all variations of Teckturna (Aliskiren).

ALTITUDE Study

The off label use of Medtronic Infuse(R) bone graft has been associated with severe side effects including in some cases, death.

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Medtronic Infuse(R) Bone Graft What is It?

Medtronic, Inc. and Medtronic Sofamor Danek USA, Inc. designed and marketed the Infuse(R) Bone Graft device (“Infuse(R)”) for lumbar spine surgery. Infuse(R) is a bio-engineered bone filling material containing a bone morphogenetic protein (“BMP”), and is used as an alternative to grafting a patient’s own bone.

Medical side effect concerns about Tekturna, a blood pressure drug sold by Novartis, have arisen after clinical trials were canceled due to a high number of strokes and kidney problems among diabetic patients.

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Novartis was running a trial of the drug to see if it could be useful in the treatment of diabetic hypertension. The drug maker found that Tekturna may increase the risk of non-fatal strokes, kidney problems and other health risks.

Read the Safety Warning from Novartis here. Direct Healthcare Professional Communication on potential risks of cardiovascular and renal adverse events in patients with type 2 diabetes and renal impairment and/or cardiovascular disease treated with aliskiren (Tekturna®) tablets and aliskiren-containing combination products.

The FDA is alarmed about the risk of complications with vaginal mesh used to treat pelvic organ prolapse and stress urinary incontinence. The Federal regulators are ordering manufacturers to conduct new medical studies on the surgical products’ safety.

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FDA Notice Letter Sent

The FDA sent a letter to several medical device makers recently calling for the new postmarketing studies on transvaginal mesh. Many experts believe that this is the beginning of tighter regulations designed to protect women from bladder sling problems.

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