A proposed study would examine the health effects of hydraulic fracturing (fracking) drilling on the people living closest to active natural gas wells.
DePuy Orthopaedics and its parent, Johnson & Johnson, continue to be named in lawsuits by metal-on-metal hip replacement recipients who suffered severe injuries, including elevated chromium and cobalt levels, allegedly due to recalled ASR hip implant devices. Most recently, the national law firm of Parker Waichman LLP filed suit on ...
People who smoke cigarettes before and after receiving a total joint replacement, such as a hip replacement device or knee implant, are far more likely to endure revision surgeries on those implants than people who don’t smoke.
A new study is raising more concerns about the safety of commonly used antidepressants, including selective serotonin reuptake (SSRI) inhibitor antidepressants. Investigators who conducted the study, which is published in the journal Frontiers in Psychology, posit that increased knowledge of the negative effects of SSRIs and other antidepressants could reduce ...
The U.S. Food & Drug Administration (FDA) is reviewing a new study that reported an increased risk of sudden, heart-related deaths among people using the antibiotic Zithromax (azithromycin), known popularly as Z-Pak. In a statement issued late yesterday, the FDA said patients being treated with Zithromax should not stop taking ...
A new study suggests fluids used during the hydraulic fracturing (fracking) process could migrate through underground fractures and contaminate water aquifers.
Medical device maker Smith & Nephew has reported a drop in sales of its metal-on-metal hip implant devices. According to the company, hip implant sales were down 2 percent during the first quarter of 2012, largely because its Birmingham Hip Resurfacing System suffered from an association with other metal-on-metal hip ...
A man from Tennessee has filed a lawsuit against the maker of Pradaxa, claiming that the blood thinner caused him to suffer a cerebral hemorrhage. The complaint alleges Boehringer Ingelheim Pharmaceuticals, Inc. concealed knowledge that Pradaxa can cause Serious, life-threatening bleeds, and did not warn that Pradaxa bleeding side effects ...
Actos (pioglitazone) continues to be named in lawsuits alleging long-term use of the type 2 diabetes drug caused patients to develop bladder cancer. Just last week, the national law firm of Parker Waichman LLP filed suit against Takeda Pharmaceuticals on behalf of a West Virginia man who developed bladder cancer ...
An attorney with a prominent personal injury law firm says an Actos whistleblower lawsuit filed earlier this year could strengthen legal claims alleging the type 2 diabetes medication caused some users to develop bladder cancer and heart failure.
A new report reveals that Boston Scientific is facing nearly 300 lawsuits over injuries allegedly caused by its transvaginal mesh products. According an article published online by Mass. Market, some 170 Boston Scientific transvaginal mesh lawsuits are consolidated in a … Continue reading →
The first test trials in the federal C.R. Bard Avaulta transvaginal mesh litigation will most likely start next year, according to a report from Bloomberg News. About 600 lawsuits involving Bard Avaulta transvaginal mesh products are currently pending in the … Continue reading →
A newly-published investigation from ProPublica has revealed that several questionable types of medical devices, including DePuy Orthopaedic’s recalled ASR hip implant, managed to make it to market without much scrutiny on the part of the U.S. Food & Drug Administration … Continue reading →
A group of Canadian women has filed a class action lawsuit against Johnson & Johnson alleging the company’s transvaginal mesh devices caused them to suffer serious, life-altering injuries. The transvaginal mesh lawsuit further alleges that Johnson & Johnson, along with … Continue reading →
Consumer Reports is blasting the way the U.S. Food & Drug Administration (FDA) approves medical devices, citing recent problems with metal-on-metal hip implants and transvaginal mesh products as evidence of the agency’s inadequacy. As we’ve reported in the past, both … Continue reading →
Johnson & Johnson’s Gynecare Prolift transvaginal mesh device was apparently on the U.S. market for two years before the company applied for regulatory approval of the product. According to a report from Bloomberg News, the Gynecare Prolift product was brought … Continue reading →
A national law firm has filed three lawsuits on behalf of women who were allegedly injured by transvaginal mesh devices manufactured by American Medical Systems, Boston Scientific Corp. and Ethicon, Inc. According to a statement issued by Parker Waichman LLP, … Continue reading →
The Food and Drug Administration (FDA) should have the ability to reject a prospective medical device if its manufacturer attempts to get it approved based on the notion it is the same as a previous device. A number of the … Continue reading →
Three multidistrict litigations (MDL) involving transvaginal mesh lawsuits will be consolidated in a single MDL in the U.S. District Court for the Southern District of West Virginia. In an order issued February 7, the U.S. Judicial Panel on Multidistrict Litigation … Continue reading →
For the second time, four Democratic lawmakers are seeking hearings into two controversial medical devices, transvaginal mesh products and the Lap-Band surgical weight loss device. The group, led by U.S. Representative Henry Waxman of California, asserts that both transvaginal mesh … Continue reading →