Benicar Lawsuit Settlement

Following several years of litigation, a Benicar settlement was announced by the makers of the popular blood pressure drug on August 1, 2017, offering financial compensation for certain individuals who experienced gastrointestinal problems, such as:

Sprue-like Enteropathy (“SLE”)
Collagenous Sprue
Unclassified Sprue,
“Celiac-like” Enteropathy (“CLE”)
Chronic Diarrhea
Nausea, Vomiting and Weight Loss
Villous Atrophy
Misdiagnosis of Celiac Disease Continue reading

Triad Sterile Wipes Recall

Serious Infections could have been caused by contaminated Triad Alcohol Wipes, Medical Pad, and other products

On January 3, 2011 The Triad Group issued recall of all lots of alcohol prep pads, alcohol swabs, and alcohol swabsticks after receiving complaints of potential contamination with an objectionable organism, Bacillus cereus. The recall came only after a 2-year-old toddler had died in December last after being infected with the Bacillus cereus, which resulted in multi-organ failure. Continue reading

Byetta

Byetta Associated with Fatal Pancreatitis

Byetta (exenatide), an injectable type 2 diabetes drug marketed by Amylin Pharmaceuticals, Inc. and Eli Lilly & Company, was approved by the FDA in 2005 as an adjunct to diet and exercise to improve glycemic control. Byetta is not used for treatment of patients with type 1 diabetes. The FDA issued its first warning in 2007 about Byetta being associated with acute pancreatitis. Continue reading

Chantix

Chantix May Increase Risk of Heart Attacks

Chantix (veranicline), manufactured by Pfizer, Inc., is a smoking cessation drug approved by the Food and Drug Administration (FDA) in 2006.

In 2009 in response to hundreds of reports the FDA required a “Black Box” warning to be added to Chantix side effects such as depression, suicidal thoughts, attempted suicide, and suicide.  A Black Box warning is the strongest warning the FDA can impose on a drug, short of taking the drug off the market. Continue reading

SSRIs and Birth Defects

Zoloft®, Paxil and other Selective Serotonin Reuptake Inhibitors (SSRIs) Linked to Birth Defects

Selective Serotonin Reuptake Inhibitors (SSRIs) include drugs like Zoloft®, Paxil, and Prozac that are generally used as antidepressants.

Recent studies have shown that using SSRIs while pregnant increases the risk of birth defects. These birth defects include, but are not limited to Persistent Pulmonary Hypertension (PPHN), heart, lung, abdominal and cranial defects. Continue reading

Topamax

FDA Warns That Topamax May Cause Oral Cleft Birth Defects

On March 4, 2011, the Food and Drug Administration issued a warning that the drug Topamax, the brand name for topiramate, increases the risk of birth defects such as cleft lip and cleft palate in children born to women who take the drug while pregnant. Continue reading

Transvaginal Mesh Devices

Transvaginal Mesh Devices

The transvaginal mesh is a type of medical device used to treat Pelvic Organ Prolapse and Stress Urinary Incontinence, conditions that may occur after childbirth and pregnancy.  The vaginal mesh products are manufactured by several companies, including Ethicon/Gynecare/Johnson & Johnson, C.R.Bard, Inc., Boston Scientific Corporation, American Medical Systems, and Caldera Medical.

Bard Avaulta Mesh vaginal sling product is marketed as the Avaulta Anterior and
Posterior Biosynthetic Support System.

Since 2005, more than 1,000 patients have suffered from serious complications following the placement of a transvaginal mesh device.  Recipients of transvaginal mesh/sling products may suffer from complications, including:  Continue reading