by Tony Isaacs
In a
jaw-dropping and perhaps literally
jaw-killing decision, the FDA has
just approved a new bone drug for
women that may lead to worse bones
and even cause bone death. Yes, you
read that right, Amgen's newly
approved bone drug Prolia, which is
designed to lower the risk of
fractures in post-menopausal women,
may also carry a significant risk of
actually causing bone death of the
jaw and weaker, more brittle bones
that it was designed to prevent. And
that isn't all of the bad news.
The new drug is designed to address
bone resorption and bone formation,
which is a natural and essential
process that rebuilds bone structure
by removing old bone components (resorption)
and replacing them with new ones via
bone formation. High estrogen levels
in post-menopausal women frequently
interfere with the body's ability to
form new bone material. As a result,
such women often have weak, brittle
bones and higher susceptibility to
breaks and fractures.
Prolia is a so-called monoclonal
antibody - a lab-produced antibody
that inactivates the body's
bone-breakdown mechanism. Like
biophosphate bone drugs, Prolia
targets the body's ability to break
down bone components. Prolia does
this by targeting a chemical signal
in the body called RANK ligand,
which is an essential part of the
body's natural process for breaking
down bones. The idea is that by
slowing the process down, bones will
lose less bone mass and be less
brittle. While the idea looks good
on paper, it can be fraught with
danger in actual practice.
A WebMD article described the way
Prolia works: "The drug slows the
bone-breakdown process -- but also
slows the entire bone-remodeling
process. Over the long term, it's
not yet clear what this will mean."
The problem is that suppression of
bone breakdown may lead to bone
formation outstripping bone
breakdown, and as has happened with
Fosamax and other biophosphate bone
drugs. With the other bone drugs,
new bone formation often produces
unnatural bone growth and results in
bones that are actually more
susceptible to fractures and
abnormalities. Even worse, the bone
drugs have caused even more
dangerous conditions, including bone
death of the jaw and spinal
paralysis.
There appear to be now assurances
that the Prolia will not lead to the
same kind of problems. As the FDA's
own press release warns, ""Prolia
causes significant suppression of
bone turnover and this suppression
may contribute to the occurrence of
osteonecrosis of the jaw, a severe
bone disease that affects the jaw,
atypical fractures, and delayed
fracture healing."
Osteochronosis, which literally
means "bone death", is one of the
more severe side effects that have
been reported for other bone drugs.
And, as if bone death of the jaw
were not enough of a concern,
several disconcerting side effects
were observed in Prolia's clinical
trials.
As WebMD reported, "In clinical
trials, women taking Prolia had a
higher risk of serious infections
leading to hospitalization,
including heart infections. Skin
reactions such as dermatitis,
rashes, and eczema also were
reported."
Some of the other side effects
included:
Back pain
Pain in the extremities
Musculoskeletal pain
High cholesterol levels
Urinary bladder infections
Prolia may also cause calcium
lowered levels of calcium, an
essential mineral for healthy bones.
So there you have it, the FDA has
approved and trumpeted yet another
unnatural Big Pharma drug whose side
effects may far outweigh the
benefits. What the FDA won't likely
approve or trumpet are the many
safer and less expensive natural
ways that women can beat and avoid
osteoporosis.
See for example:
"How to Beat and Prevent
Osteoporosis Naturally"
http://www.naturalnews.com/026841_osteoporosis_calcium_bones.html
and
"Calcium Alone is not Enough for
Healthy Bones"
www.naturalnews.com/028776_calcium_bones.html
Sources included:
http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm214150.htm
http://www.webmd.com/osteoporosis/news/20100602/fda-approves-prolia-for-high-risk-osteoporosis
http://hsibaltimore.com/2010/06/22/osteoporosis-drug/

Your hosts Tony Isaacs and
Luella May