Current Class Action Investigations
Currently we are investigating the following situations in which people have been injured across the country. If you have been injured while taking a drug that was later recalled, a drug or product that is under investigation for causing injury, or been injured in another situation in which you suspect there may be many other like you, consider calling us at 1-800-220-7321 to have a free conversation about your case. We will have an answer about your case, usually by the next business day.
Learn More About Accutane
Since its debut on the market in 1982, Accutane has been linked to severe depression, suicidal thoughts, and suicidal behavior in patients. It has also been linked to severe brain and heart birth defects in children born to women who were pregnant while taking Accutane.
Bextra may cause Stevens-Johnson Syndrome, Heart Attacks
The U.S. Food and Drug Administration released a Public Health Advisory on April 7, 2005, to warn the public that it has requested that Pfizer, Inc., manufacturer of the COX-2 inhibiting drug Bextra, to voluntarily recall the drug. Bextra has been linked to heart attacks, stroke, and Stevens-Johnson syndrome, a rare but serious allergic reaction that can be fatal. If you’ve experienced any of these life-threatening complications while on Bextra, call us now about your case. For more information …
Fosamax linked to Osteonecrosis (fossy jaw)
Merck’s osteoporosis drug Fosamax has been named in a lawsuit filed by a woman suffering from osteonecrosis of the jaw, a rare but debilitating and disfiguring condition in which soft tissue in the jawbone dies from infection. It is an irreversible condition. Unfortunately, simply halting Fosamax therapy may not limit your risk if you’ve been taking Fosamax. If you’ve experienced dental pain, “heavy jaw feeling,” or swelling in the jaw and take Fosamax, you may want to consult with a lawyer to protect your rights. For more information …
Guidant Defibrillators Recalled Due to Patient Deaths
As of December 21, 2005, a total of 35 clinical failures, including 5 patient deaths, have been reported in patients implanted with Guidant’s Ventak Prizm 2 and Contak Renewal defibrillators. The units can develop a short circuit, which could lead to cardiac arrest and death in patients with the implants. The devices are supposed to …
Ortho Evra Birth Control Patch - Blood Clots and Strokes
Some women who have worn the Ortho Evra birth control patch have suffered severe, debilitating and long-term side effects as a result, including blood clots, migraine headaches, and strokes. At least one woman has died while on the patch, and the patch may be linked to 10 other deaths according to an Associated Press investigation (July, 2005). Ortho McNeil …
Six Women Dead After Taking Mifeprex/Misoprostol “Abortion Pill”
Over 600 adverse events involving the Mifeprex/Misoprostol regime have been reported to the FDA (Source:Newsinferno.com, March 18, 2006). There is concern that adverse events may be underreported because the FDA has not made a causal link between the drug and the fatal infections of women. If you know of someone who died after taking the abortion pill regime of Mifeprex and Misoprostol, you may want to discuss your case with a lawyer. The Law Offices of James Scott Farrin is experienced in wrongful death cases. Call or contact us today for a free conversation about your situation. There is never any obligation to hire our law firm.
Corneal Damage from ReNu Moisture Loc solution
The CDC has confirmed 130 cases of eye infections from Fusarium keratitis, an eye infection that can cause permanent vision loss in patients. 60% of those patients used ReNu Moisture Loc contact lens solution prior to developing symptoms. Similar cases have been …
Seroquel linked to diabetic complications
Extreme hyperglycemia, or elevated blood sugar, has been reported in patients treated with Seroquel. Seroquel has also been associated with ketoacidosis (insulin deficiency), coma or death, all stages of metabolic dysfunction common in untreated type 1 diabetes mellitus. If you’ve been diagnosed with diabetes while taking Seroquel, you may be entitled to damages for your injuries. For more information …
Trasylol (aprotinin) Linked to Kidney Failure - Heart Attack - Strokes
Trasylol (aprotinin) is a clotting agent injected during coronary artery bypass surgery to prevent excessive blood loss. A study published in the New England Journal of Medicine in January 2006 found that administration of trasyslol at least doubles the risk of kidney failure and stroke in cardiac patients and raises the risk of heart attack or heart failure by 55%. As many as 10,000 people may now be on dialysis as a result. If you have suffered any of these injuries after being injected with trasylol during coronary artery bypass surgery, you deserve the counsel of an experienced legal team.
Viagra linked to Vision Loss
Viagra is the most popular pill in the U.S., according to its manufacturer, Pfizer, Inc. Viagra has long been known to cause visual side effects and has now been linked to NAION, a “stroke of the eye” that causes permanent loss of vision.
Vioxx doubles risk of stroke and cardiac death
Have you or a loved one recently suffered from a heart attack or stroke? Merck & Co. announced on September 29, 2004, that they are recalling Vioxx, a prescription drug commonly used to relieve arthritis and menstrual pain. Merck recalled Vioxx on September 29, 2004, due to information it released from a three-year clinical trial. The study found …
