This week, Johnson & Johnson etched its name in the history books of another big pharma company that has been fined over billions of dollars due to a drug manufacturer practices of improper marketing and failure to warn. Johnson & Johnson pled guilty to...
Fosamax Osteoporosis Drug
California Supreme Court Victory for Generic Fosamax Users
On September 25, 2013, the California Supreme Court denied the generic Fosamax manufacturers petition for review thereby upholding the June 13, 2013 Court of Appeal decision allowing people injured by generic Fosamax to go forward in the Courts and hold the generic...
Appellate Court Victory for Generic Fosamax Users
In a major victory for consumers who used the generic form of Fosamax, (Alendronate sodium) on June 13, 2013 the California Court of Appeal, Fourth Appellate District, Division Three ruled that people who used the generic Fosamax were not preempted by Federal law and...
Are Too Many Doctors Simply Sales People for Big Pharma?
Big Pharma paid doctors more than $1 billion in 2012 to act in various spokesperson capacities, for travel and meals, as well as research and royalties, which is significantly more than reported in 2011. According to a new data reported in the Financial Times, that...
Who is Responsible for J&J’s DePuy ASR, Pinnacle, Ethicon’s Gynecare, and Merck’s Vioxx and Fosamax?
Consumers injured by defective devices face an armada of attorneys as they seek to hold accountable device makers such as J&J’s hip implants DePuy ASR, DePuy Pinnacle, J&J’s transvaginal mesh product Ethicon, and Merck’s FOSAMAX that has left countless post...
New Jersey Fosamax Femur Fracture Trial Update
Glynn v. Merck Sharp & Dohme Corp. (3:11-cv-05304, U.S. District Court, District of New Jersey) started trial in April 2013. Evidence was presented from internal documents and experts from both sides as to the benefits and risks of Fosamax. The jury was asked to...
Medical Device Reporting for People Injured by Vaginal Mesh, Actos, Fosamax, and DePuy ASRs: What the Consumer Needs to Know
Manufacturers, user facilities and importers of medical devices are mandated to submit certain adverse events to the U.S. Food and Drug Administration [FDA]. Medical device reporting requires that manufacturers report to the FDA when they learn that one of their...
Fosamax Again linked to Rare Thigh Fractures
A new study published May 21, 2012 on line by the Archives of Internal Medicine said it found a link between bisphosphonate use (one of which is Fosamax) and atypical thigh fractures. Fosamax, Used to Treat Osteoporosis, Is Linked To Unusual Bone Fractures in The...
Another Blockbuster Fine, Consumers Shut Out Again
Merck, makers of VIOXX and FOSAMAX among other drugs, agreed to pay $950 million to settle criminal and civil claims that it illegally promoted the drug VIOXX. Merck will plead guilty to a misdemeanor offense and pay $321,636, 000 criminal fines. According to the...
FDA Advisory Panel Suggests Additional Warnings for Label
About 11% of women 55 years of age and older take drugs containing bisphosphonates (including Fosamax, Aclasta, Actonel, Altevia, and Boniva) to treat and prevent osteoporosis. This drug has been under increased scrutiny since a link was suspected between long term...