The FDA lowered the maximum dose of the antidepressant citalopram hydrobromide (Celexa) from 60 mg per day to 40 mg per day, after concerns that higher doses of the medication increase the risk for ...
WASHINGTON, Aug 24 (Reuters) - U.S. drug regulators warned doctors and patients against using high doses of Forest Laboratories Inc's antidepressant Celexa or its generic versions because of heart ...
AD lowers risk of cancer in older people Cognitive and cardiac adverse effects may limit the antidepressant's use for this purpose. HealthDay News — The antidepressant citalopram (Celexa) combined ...
Federal health regulators are warning doctors not to prescribe high doses of the antidepressant Celexa, because of the risk of fatal heart complications. The Food and Drug Administration said in an ...
This study showed that approximately one third of the patients who had not responded to treatment with at least 20 mg of citalopram for at least 6 weeks achieved remission (MADRS ≤8) during the 34 ...
On April 20, the FDA approved a revision to the safety labeling for citalopram hydrobromide and escitalopram oxalate (Celexa and Lexapro, respectively, made by Forest Laboratories) in tablet and oral ...
March 28 (Reuters) - U.S. health regulators added new warnings to the label of Forest Laboratories Inc's antidepressant Celexa and its generic versions about a potential risk of rare heart diseases.
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