Defective Drugs

Tulsa Dangerous Drug Lawyers, Oklahoma Drug Lawyers, Fluoroquinolones, black box warnings, FDA warning label revision, oklahoma dangerous drug lawyers, tulsa defective drug law firm, tulsa drug injury lawyers, oklahoma drug injury lawyers

FDA Strengthens Warning Labels on Class of Antibacterial Drugs

The Food and Drug Administration (FDA) announced on Tuesday, 7/26 that they are revising their boxed warning labels on packages of a class of antibacterial drugs known as fluoroquinolones. The FDA’s boxed warning labels, commonly referred to as “black box” warnings, alert doctors and patients that certain types of drugs or medical devices may pose […]

July 29th, 2016 Read More
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FDA Strengthens Warnings of Severe Kidney Injuries Caused by Diabetes Medication Invokana

The Food and Drug Administration just issued another Drug Safety Communication alerting doctors and patients about serious health risks associated with several type 2 diabetes medications, including Invokana. The FDA is strengthening warnings about the risk of serious, acute kidney injuries for patients taking type 2 diabetes medications canagliflozin (Invokana, Invokamet) and dapagliflozin (Farxiga, Xigduo […]

June 14th, 2016 Read More
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Heartburn Drugs Are Linked to Several Dangerous Side Effects

Proton-pump inhibitors (PPIs) are drugs used to reduce the body’s production of gastric acid. PPI drugs, including Prilosec, Nexium, Prevacid and others, are some of the most widely prescribed medications in the U.S, generating up to $14 billion in annual sales. Recent studies have shown that these medications are also linked to dangerous side effects […]

June 8th, 2016 Read More
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FDA Issues Safety Warning for Zecuity Migraine Patch, Warns of Burn and Scar Risk

The Food and Drug Administration (FDA) is warning consumers that a medical device used to treat migraine headaches may cause serious injuries. The Zecuity Patch uses the drug sumatriptan to treat the symptoms of acute migraine headaches. The patch is designed to be worn on the thigh or upper arm for periods of up to […]

June 3rd, 2016 Read More
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FDA Warns Patients Against Purchasing Herbal Weight Loss Supplement Containing Banned Substance

The Food and Drug Administration announced on Thursday, October 1st that consumers should avoid purchasing “Ultimate Herbal Slimcap,” a dietary weight loss supplement that was found to contain a banned substance among its active ingredients. This product is currently being marketed over the internet to consumers as a safe and effective way to aid in […]

October 6th, 2015 Read More
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FDA Adds New Warning Labels to Diabetes Medication Invokana, Citing Increased Risk of Bone Fractures In Addition to Previous Warning of Ketoacidosis

Type II Diabetes is a very serious medical condition that impacts millions of Americans. The Center for Disease Control (CDC) estimates that as many as 29 million Americans are currently living with some form of Diabetes. Unlike Type I Diabetes, many people with Type II Diabetes may be able to control their blood sugar levels […]

September 16th, 2015 Read More