Fosamax Adverse Effects

Because Merck failed to change the side effects warnings for Fosamax adverse effects in a timely
manner, lawsuits are being filed against the drug company by Fosamax users who
have developed osteonecrosis of the jaw, which is an irreversible condition. The
Fosamax lawsuits allege that Merck concealed what it knew about Fosamax adverse effects causing
osteonecrosis of the jaw from patients and their doctors -- which is similar to
what Merck previously did with its infamous painkiller, Vioxx, a couple of years
earlier.fosamax lawsuit
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• Sunday, 11 November 2007, 5:25pm GMT • 46.6k
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For almost a year, Merck & Co. failed to warn
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associated with its osteoporosis drug Fosamax (alendronate). In August
2004 the FDA's Office of Drug Safety issued its Postmarketing Safety Review
report about Fosamax -- an osteoporosis drug made by Merck & Co. --
as well as three other bisphosphonate drugs: Zometa; Aredia; and, Actonel. The
August 2004 FDA report concluded that the label, or package insert, for
Fosamax should be revised to include a warning about osteonecrosis, a
rare but serious Fosamax adverse effects observed in some
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There has been increased attention over the past couple of years given to the
association between the use of oral bisphosphonates such as Fosamax and the
Fosamax adverse effects osteonecrosis of the jaw (ONJ). It is understandable,
therefore, that Fosamax adverse effects patients want to know the early signs and symptoms of
ONJ, which is sometimes referred to as jaw bone decay. Furthermore, the
unfortunate patient diagnosed with this type of osteonecrosis should know how
the extent of their condition determines the staging of ONJ upon diagnosis as
well as their course of treatment thereafter.
More Studies Implicate Fosamax with Femur Fractures:
Fosamax lawsuit
Fosamax Bone Break femur and Thigh
A study done by Columbia University investigated 111 women taking bisphosphonates including Fosamax. Their studies demonstrated that early on in therapy patients showed marked improvement in bone structure but after long-term use bone structure diminished. Further studies conducted at the Hospital for Special Surgery in New York observed 21 women who had femur fractures. Twelve of these patients who had been on bisphosphonates for over eight years demonstrated reduced bone mass as compared to the
other 9 patients who did not take bisphosphonates. Additionally, the Annals of Internal Medicine reported that bisphosphonates like Fosamax behave more like a bone hardener than a bone builder. They have also observed that bone becomes brittle over time with the use of Fosamax.
On March 2010, the FDA began a safety review of Fosamax to determine whether or not there is an increase in the risk of bone fractures. The agency is investigating the possible link between Fosamax and fractures that occur below the hip joint on patients who have been on bisphosphonates for several years. The investigation is still on going but the FDA suggests that for patients who are currently on bisphosphonates should continue therapy but should make sure they talk to their healthcare providers
if they develop any symptoms.
If you have experienced a Fosamax femur fracture or any other bone related illness while on Fosamax, you may be entitled to financial compensation for pain and suffering, lost wages and medical expenses. You might want to speak with a Fosamax attorney to see if you qualify for a Fosamax lawsuit. Fosamax lawsuits are currently being filed across the country.