New Warning for Attention Deficit Drugs
AP
WASHINGTON (Feb. 21) - Drugs prescribed to treat attention deficit hyperactivity disorder will include guides to alert patients and parents of the risks of mental and heart problems, including sudden death
Karen Elshout, St. Louis Post-Dispatch / MCT
A patient takes part in a study on attention deficit hyperactivity disorder. The FDA ordered manufacturers to warn patients that ADHD drugs carry risks, including sudden death. Jump Below: Drug List | Talk About It: Post Thoughts
The Food and Drug Administration said Wednesday that it directed the manufacturers of Ritalin, Adderall, Strattera and all other ADHD drugs to develop the guides. In May 2006, the agency told manufacturers to revise the labels of the drugs to reflect concerns about the cardiovascular and psychiatric problems. Draft versions of the guides posted on the FDA Web site include discussion of reports of increased blood pressure and heart rate in ADHD patients, as well as cases of sudden death in some who have heart problems and heart defects. In adult patients, the reported problems also include stroke and heart attack. The alerts also cover psychiatric problems, such as hearing voices, unfounded suspicions and manic behavior, of which there is a slightly increased risk in patients who take the drugs, the FDA said. The guides also tell patients and their parents of precautions they can take to guard against the risks. Affected Drugs
The FDA announced its order applies to 15 drugs: Adderall Tablets
· Adderall XR Extended-Release Capsules
· Concerta Extended-Release Tablets
· Daytrana Transdermal System
· Desoxyn Tablets
· Dexedrine Spansule Capsules and Tablets
· Focalin Tablets
· Focalin XR Extended-Release Capsules
· Metadate CD Extended-Release Capsules
· Methylin Oral Solution
· Methylin Chewable Tablets
· Ritalin Tablets
· Ritalin SR Sustained-Release Tablets
· Ritalin LA Extended-Release Capsules
· Strattera Capsules