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Sort by date 1,437 pages found matching black box- Cipro Antibiotic Linked to Neuropathy
Cipro, an antibiotic used to fight infections, has been linked to serious side effects, including an increased risk of Cipro Neuropathy . Other Cipro side effects reportedly include an increased risk of liver toxicity and an increased risk of Cipro tendon ruptures . Cipro (generic name Ciprofloxacin, also known as Ciproxin and Ciprobay) is used... - Topps Beef Recall E. Coli Contamination Lawsuit
Nearly 21.7 million pounds of ground beef and related products suspected of E.coli contamination has been recalled by Topps Meat Company of Elizabeth, New Jersey. The suspected beef is known to have sickened 25 people in eight states so far. Of those, three are known to have contracted E.coli from the beef, with a further 22 reports under investigation. ... - Dietary Supplements Recalled Nationwide due to Undeclared Drug Ingredient
Universal ABC Beauty Supply has issued a nationwide recall of dietary supplement products found to contain the undeclared drug ingredient Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The dietary supplements listed below are not supposed to contain Sibutramine. The FDA has not approved these products,... - Reglan FAQ
What is Reglan? Reglan, known generically as metoclopramide, is approved by the US Food and Drug Administration (FDA) for the treatment of Symptomatic Gastroesophageal Reflux Disease (GERD) and Diabetic Gastroparesis. It is also used to treat nausea caused or brought on by cancer chemotherapy treatment. Reglan is not approvedâthat is, Reglan is c... - Reglan side effects | Side effects of Reglan | Lawyersandsettlements.com
Reglan (metoclopramide) is used to treat Gastroesophageal Reflux Disease (GERD), acid reflux disease and heartburn. While many Reglan side effects are minor, some patients have experienced serious side effects, including Tardive Dyskinesia . Some metoclopramide side effects, such as Neuroleptic Malignant Syndrome , can be fatal while others are permanent... - Asthma Medication Deaths: Serevent, Advair, & Foradil - Asthma Lawyer & Case Evaluation
In February, 2010, the US Food and Drug Administration (FDA) issued a warning about the risk of certain Asthma inhaler side effects . There is now a Serevent and an Advair black box warning , alerting patients to the risk of using those medications. Furthermore, patients are warned to be on the alert for Foradil side effects, which can include worsened bre... - Tyson Foods Recalls Chicken Breast Products
Products May Contain an Undeclared Allergen, Soy Tyson Foods, Inc, a Vicksburg, Miss. establishment, is recalling approximately 51,360 pounds of raw frozen chicken breast tenderloin products because they may contain soy, which is not declared on the label. The following products are subject to recall: 10-pound cases of "Standard Quality Unco... - There could be E. coli in your Hamburger: Topps Recall
Sep-29-07 Elizabeth, NJ Hamburgers possibly contaminated with E. coli have sickened eight people in eight states, and has resulted in a recall of frozen hamburger , according to a release by the Centres for Disease Control and Prevention (CDCP) in Atlanta. On Tuesday the Topps Meat Company, based here, recalled 331,582 pounds of frozen beef patties as well as... - Elmiron Vision Loss Lawsuit news and Legal Information
Elmiron (pentosan polysulfate sodium), a drug widely prescribed for a bladder condition, has been associated with eye damage. Hundreds of thousands of people who have taken Elmiron may have been exposed to the risk of potentially permanent vision damage. Recent studies suggest that Elmiron is toxic to the retina, and one study shows that about 25 percent o... - Uloric Black Box Warning Legal News and Lawsuit Information
The FDA issued a black box warning for the gout medication Uloric (febuxostat) in February 2019 after results of a clinical safety study found an increased risk of heart-related death and death from all causes compared to other drugs to treat gout. Uloric lawsuits claim that Takeda, the manufacturer of Uloric, failed to warn users of the increased risk of he... - Aranesp, Epogen, & Procrit Lawsuit News and Legal Information
Aranesp, Epogen, and Procrit -- three common drugs used to treat anemia -- have been linked to serious complications in cancer and kidney patients. The drugs, which are erythropoiesis stimulating agents (ESAs), have been approved to treat anemia in patients with chronic kidney failure and in cancer patients whose anemia is caused by chemotherapy. Epogen... - Avelox Antibiotic Injuries Lawsuit News and Legal Information
Avelox (moxifloxacin hydrochloride), is in a class of antibiotic drugs known as fluoroquinolones, which includes Cipro and Levaquin. Avelox antibiotic is used to fight bacterial infections and is generally prescribed to treat bacterial sinusitis, chronic bronchitis, and community-acquired pneumonia. However, the oral fluoroquinolones have been linked to... - Botox Linked To Paralysis & Death
On August 3, 2009 the FDA updated its safety alert to a Black Box Warning on the popular anti-wrinkle drugs Botox and Myobloc . All Botox product labels now warn that the effects of the botulinum toxin may spread from the area of injection to other areas of the body, causing symptoms similar to those of botulism. Those symptoms, which have mostly been see... - Avandia: A New Black Box Warning, and a Reprieve from the FDA
Nov-18-07 Washington, DC As some had predicted, GlaxoSmithKline caved to sustained pressure by the US Food and Drug Administration (FDA) and agreed to add a second black box warning for Avandia , the diabetes drug linked to increased risk of heart attack. However, the warning is somewhat watered-down, and in the absence of any unforeseen, blockbuster medical r... - Avandia vinculado con ataques cardíacos y lesiones hepáticas
Avandia: Casos verídicos y entrevistas Avandia asociado a insuficiencias cardíacas: ¿Avandia provocó el ataque cardíaco de esta mujer? Karen Trelford quedó anonadada tras ver el informe en la televisión, este verano, que denunciaba que el medicamento contra la diabetes Avandia presuntamente expon&iacut... - National Black Farmers Association Joins Monsanto MDL
Apr-27-21 San Francisco, CA On April 1, the Judicial Panel on Multidistrict Litigation denied Monsanto Company’s request that it reconsider its decision to include National Black Farmers Association v. Monsanto Co. in the Multidistrict Litigation (MDL), consolidated in the Northern District of California. National Black Farmers Association, a Monsan... - Black & Decker Recalls Cordless Electric Lawnmowers
Washington, DC: Black & Decker US Inc, is recalling about 160,000 (these lawnmowers were previously recalled in September 2002 for a fire hazard, and that recall was expanded in August 2006), because the lawnmower's motor and blade can unexpectedly turn on after the mower's safety key is removed, posing a laceration hazard to consumers. Removing the... - Google Slammed with Another Discrimination Lawsuit
Mar-24-22 San Jose, CA Google has been slammed yet again with a lawsuit alleging a pattern of racial discrimination against Black and minority employees. Filed in U.S. District Court for the Northern District of California in San Jose and seeking class-action status, the plaintiff accuses Google of systematic discrimination against Black workers by placing th... - Reports of Injury Prompt Black & Decker Sanders Recall
Washington, DC: Black & Decker is recalling roughly 192,000 Black & Decker Random Orbit Sanders because the black plastic disc (called the platen) that holds the sandpaper can fly off or break apart during use and the disc, or pieces of the disc, can hit the user or those nearby, posing a laceration hazard. Black & Decker has received 73 reports... - FDA Orders Changes to Ketek but Leaves It on the Market
Mar-26-07 Rockville, MD: The U.S. Food and Drug Administration (FDA) is making changes to the labeling of Ketek following pressure from numerous organizations regarding the drugs' safety. The organization has announced that Ketek will now come with a black box warning to alert consumers to the potential for serious side effects associated with taking the drug. ...