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Fruta Planta® Lawyer & Lawsuit
In October 2010, the U.S. Food & Drug Administration in association with Godi International, Corp. and PRock Marketing LLC announced a nationwide recall of the Fruta Planta weight loss dietary supplement after receiving reports of serious, life-threatening cardiac complications and one death. If you or a loved one has been injured by Fruta Planta,…
Federal Bard Vaginal Mesh Trials to Begin Feb. ’13
C.R. Bard Inc. is scheduled to face its first federal court trial early next year over allegations that the company’s transvaginal mesh (TVM) devices injured recipients. A trial date of Feb. 5, 2013, has been set for the first of approximately 600 federal lawsuits alleging that Bard’s Avaulta implant caused severe organ damage. U.S….
Oral Sodium Phosphate (OSP) Lawyer & Lawsuit
Oral Sodium Phosphate medications used prior to colonoscopies have been linked to serious, life-threatening kidney injuries and/or kidney failure. These kidney problems are also known as acute phosphate nephropathy. If you or a loved one has been injured by an OSP, you should contact our lawyersimmediately for a free confidential case evaluation. You may…
OsmoPrep® Lawyer & Lawsuit
A large number of colonoscopy patients have suffered from serious kidney damage (acute phosphate nephropathy) after using OsmoPrep bowel cleansing product. Given the serious nature of the injuries consumers were reporting, in 2008 the FDA required a black box warning be added to the labeling of this product. If you or a loved one…
Popular Birth Control Pills Given Revised Warning Labels
Birth control pills that contain drospirenone, otherwise known as fourth generation oral contraceptives, have recently become the subject of increasing distain within the healthcare community. Reports indicate that the use of such contraceptives may coincide with catastrophic complications. Of significant concern, however, is their recent association with the development of severe, life-threatening blood clots….
Victoza® Lawyer & Lawsuit
Victoza (generic: liraglutide) was approved by the U.S. Food and Drug Administration (FDA) to serve as a once-daily injection for the treatment of type 2 diabetes in some adults. Of significant concern, however, are the serious side effects that have recently been associated with clinically relevant Victoza exposure. Subsequently, Victoza treatment may place patients…
New Study: SSRIs May Be Responsible For a Twofold Increase In PPHN
Recent years have witnessed several antidepressant medications become the subject of increasingly critical skepticism. Compounding the criticism further are reports of new evidence that lends weight tot he long-suspected link between selective serotonin reuptake inhibitors (SSRIs) and congenital birth defects. According to a new study, the risk of a child developing persistent pulmonary hypertension…
Topamax® Side Effects
The U.S. Food & Drug Administration (FDA) has recently strengthened their initial warning on the drug Topamax (generic: topiramate). Previously, the Topamax medication was assigned to the Pregnancy Category C because of a lack of human data. However, they strengthened the warning to Category D as a direct result of new data that suggests…