Voltaren Gel is misleading?
April 19, 2010
THE US Food and Drug
Administration has issued a warning
letter to Novartis Consumer Health,
regarding what it sees as “false or
misleading” direct-to-consumer
Voltaren Gel information.
According to the FDA, Novartis’
direct-to-consumer Voltaren Gel
promotional materials breached
several statutes in the US Food and
Drug Act, by overstating the
product’s efficacy and also by
minimising “serious risks”
associated with Voltaren’s usage.
The direct to consumer email in
question claimed that Voltaren Gel
“[keeps] joint pain from interrupting
your days ahead” and “[keeps you]
living life with less painful interruptions”.
The FDA took umbrage at the
claims, saying they imply that
Voltaren Gel has been proven to
have a “direct, positive, and broad
impact on a patient’s activities of
daily living by reducing or
eliminating daily interruptions due
to joint pain”.
The “FDA is not aware of
substantial evidence or substantial
clinical experience demonstrating
that using Voltaren Gel results in an
overall positive impact on the
general activities of daily living as
suggested,” the agency said.
The FDA also found Novartis’
claims that Voltaren provides
“targeted relief” were misleading
because it suggested that Voltaren
may be useful on any type of joint
pain, whereas in fact it has only
been FDA indicated for “relief of
the pain of osteoarthritis of joints
amenable to topical treatment, such
as the knees and those of the hands”.
Novartis also received a warning
over the minimisation of usage risks
because the risks were presented
“in extremely small black font, and
in [difficult to read] single-spaced
paragraph format” and in “complex
medical terminology”.
The FDA has now ordered Novartis to
cease the distribution of all of the
offending promotional materials,
and has also requested a written
response as to whether the
company will comply, and exactly
which other promotional materials
contain the same “misleading” and
“false” information.
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