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Fosamax Lawsuit

Levin, Papantonio shareholder Tim O'Brien informs the Fosamax Examiner that closing arguments are set for Tuesday, April 17, in the New Jersey Fosamax bellwether trial in the case of Jo Ann Sessner vs. Merck & Co.. The case involves the claim of a Florida Fosamax patient who developed Stage 3 bisphosphonate-related osteonecrosis of the jaw after more than six years of Fosamax use. Read More
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LEVIN PAPANTONIO APPOINTED TO LEAD FOSAMAX CASE

Firm Attorney Timothy O'Brien has been appointed Lead Counsel by the United States District Court for the Southern District of New York in MDL No. 1789In re Fosamax Products Liability Litigation. Mr. O'Brien concentrates his practice in the areas of product liability, personal injury, wrongful death, and mass tort litigation. He has previously been appointed as discovery co-chair in In re Accutane Products Liability Litigation., MDL No. 1626, as discovery co-chair inIn re Medtronic, Inc., Implantable Defibrillators Product Liab. Litig.,MDL No. 1726, as a member of the Plaintiffs Steering Committee in In re Guidant Corp. Implantable DefibrillatorsProduct Liab. Litig.,MDL No. 1708, and served on the discovery committee of In re Phenylpropanolamine ("PPA") Product Liab. Litig.,MDL No. 1407. As the lead attorney responsible for Levin Papantonio's PPA litigation, he has secured over $20 million in settlements for the firm's clients. He has taken the national lead in prosecuting Fosamax osteonecrosis of the jaw cases and has been interviewed and extensively quoted in The Wall Street Journal, New York Times, The Associated Press, Bloomberg News, and by National Public Radio, CBS Radio, and Air America Radio.

Levin Papantonio is investigating claims and Fosamax lawsuits nationwide for Fosamax users who have suffered damage to their jaw bone as a result of the popular medication. If you have been injured by Fosamax, Actonel , Aredia, or Zometa, contact our Fosamax Attorneys for a free legal consultation. You may be entitled to compensation for a jaw bone injury which could have been prevented.

~ ON THE AIR ~
FOSAMAX

Mike Papantonio, co-host of Air America Radio's Ring of Fire, interviews Levin Papantonio partner Tim O'Brien about the drug Fosamax and how it can cause the jawbone to rot and die.

Fosamax is taken by millions of Americans to strengthen bones.

Listen to the Fosamax Interview

National Public Radio Investigative Story:

Merck Pushes Fosamax on Women without Any Illness

Listen to the Biography

Related Articles

  • Follow the Fosamax Blog (Updated!)

    Keep up to date with all of the latest news, links, and opinions on the Fosamax Blog hosted and edited by Levin Papantonio attorney Tim O'Brien.
  • Coast to Coast Radio Program: Fosamax - Is it the next VIOXX?  

    Find out more about personal injury lawsuits and class actions being filed against Merck by women who took the drug, Fosamax. Many now suffer severe medical and dental problems. Co-hosts & Attorneys J. Craig Williams and Robert Ambrogi explore what's going on with Fosamax with the lawyer taking the lead nationwide in Fosamax litigation - Attorney Tim O'Brien at the firm of Levin, Papantonio,Thomas, Mitchell, Ecshner & Proctor in Pensacola.
  • Bone-building drugs linked to bone-rotting side effect - The Star Ledger

    The New Jersey Star Ledger examines Fosamax and interviews Tim O'Brien on Merk's marketing push and lack of warnings to doctors on potential side effects.
  • Fosamax lawsuit brings risks to light

    Fosamax: Bone-building med linked to jaw decay in dental patients, a fact Merck is accused of veiling.

In The News

A New England Journal of Medicine study recently published indicates that less than 10% of women with normal, mild, or moderate T-scores will develop osteoporosis over a fifteen year period. This study calls into question the currently Medicare DEXA-scan screening protocol of every two years for postmenopausal women. Further, because most osteopenic women never would develop osteoporosis, the study refutes marketing positions adopted by Merck & Co. relating to its prescription drug Fosamax which Merck touted would help osteopenic women prevent osteoporosis. Read More
In September 2011, Chief Judge Garrett Brown of the United States District Court for the District of New Jersey announced his upcoming retirement from the federal bench.  Chief Judge Brown was the judge assigned by the Judicial Panel on Multidistrict Litigation ("JPML") to oversee the Fosamax Femur MDL pending in the District of New Jersey.  As a result of Judge Brown's announced retirement, the JPML reassigned the Fosamax Femur MDL to District Judge Joel Pisano, effective November 22, 2011.  Like Chief Judge Brown, Judge Pisano sits in Trenton, NJ.&nb Read More
The Wall Street Journal reports that Merck & Co. has been issued a criminal investigation subpoena by the U.S. Department of Justice regarding how Merck marketed its brain tumor medication, Temodar; its hepatitis C drug, PegIntron; and its cancer treatment, Intron A.  In an August 2011 filing with the Securities and Exchange Commission, Merck disclosed the subpoena as part of a “federal health-care investigation under criminal statutes”.  Read More
ADELPHI, MD At today's FDA Panel conference on the long term use of osteoporosis drugs like Fosamax, presenter Arthur C. Santora MD, PhD, speaking for Merck, the drug manufacturer, attempted to convince the panel that limits on the duration of the drugs use were not necessary. However, Dr. Santora did admit that drug "holiday" (meaning a temporary interruption in usage) may be considered for patients who are no longer considered to have a sufficiently high fracture risk. Read More
ADELPHI, MD In the early morning session of today's FDA Panel conference on the long term use of bisphosphonates, like the drug Fosamax, the FDA's Lead Medical Officer Fatmatta Kuyateh, M.D. indicated that radiographic findings consistent with atypical femur fractures case have been associated with bisphosphonate use. Read More
A review of Merck's public filings reveals that Merck has spent more than $150 million litigating approximately 1,500 cases involving Fosamax patients who developed bisphosphonate-related osteonecrosis of the jaw after taking Fosamax. This figure is certainly striking given the relatively small number of cases in litigation and given the fact that, of the 1,500 cases, Merck has only done active discovery in less than 50 of the cases. Read More
Fosamax has long been known to have an incredibly long terminal half-life in bone.  Merck, the manufacturer of Fosamax, has conducted clinical trials which show that the the half-life of Fosamax in bone is 10.9 years.  Despite Fosamax's well established long half-life in bone, Merck insists that the biologic effects of Fosamax quickly dissipate after the last pill is taken.  Recently published research, however, shows that Merck's claim of "no lingering effect" is unfounded.  In the July 2011 edition of the medical journal BONE, meta Read More
The International and American Association for Dental Research has published a major prevalence study and a major case control study showing that the use of oral bisphosphonate drugs such as Fosamax massively increases a patient's relative risk for the development of osteonecrosis of the jaw (literally, "death of the jaw bone").  Published in the Journal of Dental Research April 2011 edition, the article "Risk Factors for Osteonecrosis of the Jaws:  a Case-Control Study" shows that Fosamax patients had an odds ratio of 12.2 for the develo Read More
NEW YORK CITY
JURY FINDS
FOSAMAX
"UNREASONABLY
DANGEROUS" AND
"DEFECTIVE"

-----------
AWARDS FLORIDA
JAW PATIENT
$8 MILLION

June 25, 2010: A seven-member jury sitting in the United States District Court for the Southern District of New York found that Merck's prescription drug Fosamax was "unreasonably dangerous" and "defective". The case, Shirley Boles v. Merck & Co., Inc., was tried by Levin Papantonio shareholder Tim O'Brien together with Gary Douglas of Douglas & London, and was a so-called bellwether trial in the Fosamax MDL involving osteonecrosis of the jaw injuries. After a three-week trial. the Court asked the jury to answer the following question: "Do you find that Fosamax was a defective product before October 1, 2003, that is, unreasonably dangerous due to defective design, and that its defective design was a legal cause of Mrs. Boles' injury?" The jury unanimously answered "YES". The jury was then asked to determine the amount of damages Mrs. Boles sustained as a result of her taking the drug Fosamax. The jury determined that her damages amounted to $8 million. In a post-verdict interview, Attorney O'Brien put his arm around the seventy-two year old retired sheriff's deputy and stated: "This is the world's bravest great-grandmother. She took on Goliath and won." View Verdict

 

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