Why the study?
What is the incidence and type of adverse cardiovascular events associated with stimulant medications prescribed for ADHD in the community setting?
What is the incidence and type of adverse cardiovascular events associated with stimulant medications prescribed for ADHD in the community setting?
This letter explores the incidence of adverse cardiovascular events associated with ADHD stimulant medications in a community setting following FDA warnings.
To the Editor: On February 9, 2006, a Food and Drug Administration (FDA) advisory panel recommended that stimulant drugs prescribed for attention deficit–hyperactivity disorder (ADHD) carry warnings about the potential for an increased risk of sudden death and cardiovascular problems such as hypertension, cardiac arrest, arrhythmias, and stroke.1 Although stimulant drugs are known to cause adverse cardiovascular effects,2,3 little is known about the incidence and type of adverse events in the community setting. To explore this issue, we examined adverse events from stimulant medications prescribed for the treatment of ADHD. We used data from the National Electronic Injury Surveillance . . .
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Cohen et al. (2006) conducted a letter in Attention Deficit-Hyperactivity Disorder (ADHD). Stimulant medications was evaluated on Adverse cardiovascular events.
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