Thursday, February 26, 2009

Forest Laboratories Accused of Fraud

The manufacturer of Celexa and Lexapro, Forest Laboratories, is in deep trouble with the US government by failing to report the negative side-effects of their drugs on children. Their studies showed that the drugs were not very effective in children and that they could lead to suicidal feelings as well.

By hiding these facts, Forest did not adequately inform the health care industry about the detrimental effects of their drugs, which is illegal. This led to doctors prescribing drugs that they did not know the whole truth about; therefore, the government is suing Forest for 3 times the amount of federal money spent on all pediatric prescriptions for Lexapro and Celexa.

In addition, Forest also used incentives such as gift certificates to restaurants and paid vacation to entice doctors to prescribe their medications. When Celexa’s active ingredient became generic in 2002 (citalopram), they marketed Lexapro, which is a different version of citalopram, an anti-depressant.

An article in the New York Times suggested that this is a common situation with many antidepressant manufacturers. Antidepressant makers try to hide the negative symptoms to further promote their drug. Most antidepressants can have negative side-effects, so doctors should take extra care when prescribing them.

Many doctors require a check up with patients several weeks to a month after prescribing the antidepressant to verify that the drug is doing its job. This is the best way to approach the problem because it minimizes potential problems caused by antidepressants. The healthcare industry is a lucrative business, but patient care must continue to be the highest priority for doctor’s in order to further benefit the health of our nation.

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