Johnson & Johnson’s Ethicon Inc. division revealed yesterday that it will end sales of its Gynecare Prolift device and three other transvaginal mesh products. The plan to stop selling the four products was set forth in a letter filed by the company in the Ethicon transvaginal mesh multidistrict litigation ...
An advisory panel for the U.S. Food & Drug Administration (FDA) began a highly-anticipated meeting yesterday to discuss the safety of metal-on-metal hip implants. Among other things, the panel of outside experts is being asked to make recommendations regarding the best practices for monitoring patients with metal-on-metal hip replacements. ...
Individuals considering undergoing knee replacement surgery should ask their doctors to run a test to determine if they have a nickel allergy. Determining if a patient suffers from a nickel allergy will ensure the right knee implant is chosen for their surgery, and possibly save them from considerable pain and ...
In a joint statement, the American Society of Clinical Oncology and the American Association for Cancer Research have called on the federal government to move quickly to regulate e-cigarettes and increase research on their health effects.
These leading research and treatment organizations asked the Food and Drug Administration (FDA) to make ...
A prominent researcher has been implicated in an alleged cover-up of Actos side effects, according to a report from TheHeart.org. An Actos whistleblower lawsuit unsealed earlier this year has alleged financial connections between the Cleveland Clinic’s Dr Steven Nissen and the maker of Actos “should be considered when analyzing Actos’s ...
Yet another study is adding to concerns about the potential dangers associated with metal-on-metal hip implants. The study, published in the Journal of Bone and Joint Surgery, found that large diameter metal-on-metal total hip replacement may be associated with a substantially higher incidence of pseudotumor formation.
A newly published metal-on-metal hip replacement study is reporting that the majority of failures occur early, within two years of surgery. The study, published in the journal Orthopedics, is just the latest to indicate that close follow-up of metal-on-metal hip implant patients is warranted.
A woman who developed inflammatory bowel disease (IBD) after taking Hoffman-LaRoche’s acne drug Accutane, has been awarded more than $1.5 million in compensatory damages and medical expenses. This was a retrial of the case; an earlier verdict was overturned on … Continue reading →
A New Jersey jury has ordered the maker of Accutane to pay a total of $18 million to two people who developed inflammatory bowel diseases while using the drug. According to a report from Bloomberg News, Roche Holding AG has … Continue reading →
A new study has associated the acne medication Accutane (isotretinoin) with an increased chance of developing some form of eye disorder. According to a report from HealthDay News, researchers at Tel Aviv Medical Center in Israel have found that people … Continue reading →
Another < "http://www.yourlawyer.com/topics/overview/accutane_ibd">Accutane trial has ended with a win for a plaintiff. The Street said that the six-week trial resulted in a $2 million award for one of three plaintiffs after their attorneys argued that Roche, the maker of Accutane, … Continue reading →
There are now 2,441 < "http://www.yourlawyer.com/topics/overview/Accutane-Side-Effects-Inflammatory-Bowel-Disease-Colitis-Crohns-Disease-Lawyer-Lawsuit-Attorney">Accutane inflammatory bowel disease (IBD) lawsuits pending in a New Jersey mass tort litigation that began five years ago. Over the fall, more than 800 lawsuits were filed in the Accutane litigation, and it is … Continue reading →
A new Accutane study out of Sweden has linked the controversial acne drug to an increased risk of suicide. The studyâ€™s findings support increased mental health monitoring of patients for up to a year after taking Accutane. Approved by the … Continue reading →
Inflammatory Bowel Disease (IBD)â€”Ulcerative Colitis and Crohnâ€™s diseaseâ€”are some of the dangerous side effects linked to Accutane. In 2005, the Accutane label was modified to warn that IBD had been associated its use; however, many believe the warning did not … Continue reading →
More than 400 Accutane lawsuits alleging the acne drug caused a variety of side effects, including inflammatory bowel disease (IBD), Crohn’s disease and ulcerative colitis, have been filed in a New Jersey mass tort litigation over the past two months. … Continue reading →
Actor John Marshall has filed suit against Roche AG, the maker of Accutane. The 43-year-old Marshall, who played U.S. Marine Louden Downey in the 1992 hit movie â€œA Few Good Men,â€ claims he developed inflammatory bowel disease, or IBD, from … Continue reading →
Roche Laboratories Inc. and Hoffman-LaRoche Inc., makers of acne drug Accutane, just settled a lawsuit that was pending for seven years. A man alleging Accutane caused his inflammatory bowel disease filed the lawsuit, said the St. Claire Record. Accutane, which … Continue reading →