When it comes to medications, it’s important to remember that there can be risks associated with taking them. And, some of the risks can be serious and even life-threatening.
Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) are among the most lethal and severe adverse cutaneous reactions, yet very little is known to most people about these conditions.
It has been six months since the Food and Drug Administration (FDA) ordered retailers to stop selling all prescription and over-the-counter (OTC) ranitidine medications, commonly known as Zantac.
Military service members thought they were protecting themselves with 3M Dual-Ended Combat Arms Ear Plugs. Unfortunately, the devices offered no protection when worn as instructed by the company.
After a thorough investigation, the U.S. Food and Drug Administration (FDA) has requested that manufacturers immediately withdraw all prescription and over-the-counter (OTC) ranitidine medications, commonly known by the brand name Zantac, from the market.
Promising weight-loss drug Belviq has been pulled off the U.S. market due to the potential risk of cancer. At the request of the U.S. Food and Drug Administration (FDA), drug manufacturer Eisai Inc. has voluntarily withdrawn and discontinued sales of Belviq (lorcaserin). The FDA took…
Childers, Schlueter & Smith is pleased to announce Ashley Spires recently joined our team. Prior to joining the firm, Ashley was a partner with a National civil litigation defense firm where she successfully litigated and tried cases in defense of nurses, doctors, medical practices, product…
Though no longer trending at the top of the news, the devastating consequences of defective hernia mesh continue to impact thousands of people in the United States on a daily basis. Hernia mesh is the net-like medical sheet used in over one million hernia repairs…
Recently, I blogged about Johnson & Johnson’s Oct. 18 recall of nearly 33,000 bottles of its baby powder, which came alongside a disclosure that a government-funded test detected traces of cancer-causing asbestos particles in a sample of the powder. The contaminated sample came from Baby…
On Nov. 4, I blogged about the Food & Drug Administration’s (FDA’s) public statement announcing the detection of N-nitrosodimethylamine (NDMA) in preliminary tests of the heartburn medication ranitidine, which is most often sold under the brand name Zantac. NDMA is a chemical agent categorized as…
On Oct. 19, the FDA announced J&J’s recall of nearly 33,000 bottles of its 22-oz Baby Powder. This came alongside a Johnson & Johnson (J&J) disclosure that a government test detected traces of cancer-causing asbestos particles in a sample of J&J Baby Powder. The recall…
