http://bmj.com/cgi/content/full/323/7310/415
BMJ 2001;323:415 ( 25 August )
Scott Gottlieb
A coalition of US consumer groups has filed a lawsuit against
Schering-Plough, the manufacturer of the allergy drug Claritin (loratadine),
claiming that the company falsely advertises the benefits of the
medicine.
The Boston based coalition, known as the Prescription Access Litigation
project, filed a class action lawsuit accusing the drug manufacturer
of misrepresenting Claritin in its advertising
causing increased demand for the
drug
and of artificially inflating its price.
The complaint alleges that Schering-Plough's advertising of the drug
falsely depicts the benefits of the drug and how effective the drug
really is.
The group filing the suit said that the advertising has made Claritin the
top selling allergy medicine in the United States. Denise Foy, a
spokeswoman for Schering-Plough, said that Claritin is the top
selling antihistamine "because it works." She disputed the
notion that the firm deceptively advertises Claritin and noted that
it follows the Food and Drug Administration's regulations on drug
advertising.
Last year Schering-Plough spent $111m (£79m) on "direct to
consumer" advertisements promoting the allergy drug, according to
the lawsuit, which said that the advertisements consistently make a
false promise that Claritin works for everyone.
In fact, medical research shows that Claritin fails to provide allergy
relief about half the time, and performs only slightly better than a
placebo, according to the lawsuit.
Prescription Access Litigation, a coalition of more than 50 consumer,
healthcare, and legal groups has filed four suits this year against
large drug companies. A suit filed in May against Barr Laboratories
and AstraZeneca alleged that the firms illegally kept a generic
version of the breast cancer drug tamoxifen off the market, forcing
patients to pay far higher costs for the brand name drug.
In a separate blow to Schering-Plough last week, another US consumer
advocacy group claimed that 17 people died because of faulty
asthma inhalers made by the company, millions of which were recalled
(from September 1999 to March 2000) over concerns that they did
not contain medicine.
Bill O'Donnell, a spokesman for Schering-Plough, said that the company had
"no evidence that a patient was ever harmed by an inhaler
subject to any recalls" and that "every inhaler returned to
the company by a patient claiming injury and alleging the canister lacked
active ingredient has been tested and found to contain active ingredient."
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