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Are all diet drugs safe?
Recent years have seen many recalls of hastily approved diet
drugs. Scheduled to be prescribed for blood sugar control in patients
with type 2 diabetes mellitus- (non-insulin dependent diabetes),
these defective products are responsible for scarring, pain, suffering,
disabilities, loss of income, debt due to medical and other bills
and even death. Unfortunately, the very patients who are receiving
these prescriptions may be least likely to tolerate them.
_ In July of 1997, the FDA requested that fen-phen, and derivations
of fen-phen, also known as redux, be recalled after reports of
neurological damage or heart failure.
_ Ephedra or Ma Huang is a diet supplement (not regulated by the
FDA). The FDA is now calling for limits on recommended dosages
and proposing new consumer notice (labeling) requirements due
to reports of heart attack, seizure, stokes, hemorrhage, high
blood pressure, rapid or irregular heart rate, or death.
_ In March 2000, Rezulin, also known as Actos, or Avandia, was
recalled in the United States due to liver toxicity and reports
of heart damage.
_ PPA or Phenylpropanolamine is used in numerous diet pills, such
as Dexatrim and Accutrim. The FDA is investigating a ban on the
use of PPA in prescription and nonprescription drugs. PPA may
be responsible for several hundred hemorrhagic strokes suffered
by people under the age of 50.
_ On Tuesday, March 19, 2002, Public Citizen, a consumer group,
petitioned the FDA to pull Meridia off the market in the United
States. Meridia, also known as Sibutramine or Reductil, was called
"unacceptably dangerous" after reports began to be received
of liver failure and deaths. (Some European countries have suspended
sales of Meridia.)
Many patients in need of weight reduction due to other serious
and possibly life threatening medical conditions, have also been
prescribed other drugs which interact with these diet drugs in
dangerous ways. A majority of patients with Type 2 Diabetes also
have hypertension (high blood pressure) and other disorders. Medications
for hypertension, Parkinson's disease, depression - even medications
over the counter for allergies and colds - have been shown to
dangerously increase medical risks of cardiac problems (including
heart failure), liver problems (including extensive damage requiring
a transplant of the liver and liver failure), eye damage, inability
of blood to clot, bruising, neurological complications and seizures.
Products' liability laws are designed primarily to prevent harm
or to compensate a person or property for harm. The harm or injury
caused by diet drugs is most often a physical injury and/or financial
injury. These laws are generally grouped under the same category
as Personal Injury Law, which is tort law.
The primary aim of tort law is to provide relief through compensation
to injured parties for the damages they have incurred. Among the
types of recoverable damages are: loss of earnings capacity, pain
and suffering, and reasonable medical expenses. They include both
present and future expected losses. This means that a person who
has been injured due to a defect in a product or a breach of an
expressed or implied warranty may be able to bring a lawsuit against
the manufacturer or the seller, or anyone else in between.
Wrongful Death is a very real possibility when diet drugs are
taken improperly or not monitored properly and the end result
is death. In these instances the law provides for compensation
to the victim's heirs or estate.
DISCLAIMER
This information has been prepared only for general purposes
and is not
legal advice. Presentation of this information is not intended
to create an
attorney client relationship. Do not act upon this information
without
seeking professional counsel.
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