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Cardiac valvular disease, pulmonary hypertension, cardiac fibrosis; [3] [23] re-approved in June 2020 for the treatment of seizures associated with Dravet syndrome, under FDA orphan drug rules. Fenoterol: 1990 New Zealand Asthma mortality. [3] Feprazone: 1984 Germany, UK Cutaneous reaction, multiorgan toxicity. [3] Fipexide: 1991 France ...
In 1984, the company acquired O'Neal Jones & Feldman for $8.8 million after a federal investigation resulted in one of its drugs being recalled. [4] [2] On July 17, 1998, the company received approval from the Food and Drug Administration for Celexa , an antidepressant. [5]
[32] and was approved for marketing in Europe in 1989. [citation needed] In October 2001 Forest Laboratories acquired the rights to market the drug in the US. [32] [33] It was approved by the US Food and Drug Administration (FDA) in July 2004. [34] The first generic versions of acamprosate were launched in the US in 2013. [35]
Originally approved for medical use in the U.S. in 1984 to treat heroin addiction and available to treat AUD since 1994, the drug binds to opioid receptors, part of the body’s system for ...
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]
Commonly prescribed thyroid drug levothyroxine was linked with bone mass and bone density loss in a cohort of older adults in a recent study. ... race, history of alcohol consumption, history of ...
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The drug was first marketed in Denmark and as of 2008, Denmark is the country where it is most widely prescribed. It was approved by the FDA in 1951. [24] [27] The FDA later approved other drugs for treatment of alcoholism, namely naltrexone in 1994 and acamprosate in 2004. [24]