Monday, February 13, 2012
Pediatric experts recommend label change for ADHD drug Focalin
An  FDA advisory panel said Novartis' Focalin should carry a warning about a risk of  suicidal thoughts in children receiving the attention-deficit/hyperactivity  disorder treatment. The agency identified eight cases of the adverse effect in  the past six years. FDA staff and advisers also recommended that Focalin's label  warn about angioedema and anaphylaxis risk. Reuters (1/30)  http://www.reuters.com/article/2012/01/30/us-fda-adhd-idUSTRE80T1WI20120130
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