The three drugs are in 20 mg tablet form, were packaged in 100 count bottles with the lot number 311756. They are:
- Dextroamphetamine Saccharate
- Amphetamine Aspartate
- Dextroamphetamine Sulfate and Amphetamine Sulfate
According to the manufacturer, Barr Laboratories, the tablets are oval and peach-colored, and have the numbers "b/973" stamped on one side and "2/0" on the other. The company distributed the affected lot between June 11, 2009 and June 16, 2009. Only lot 311756 is affected by this recall.
The risk of taking one of these drugs with too much active ingredient, according to Barr, includes: cardiovascular, neurologic, psychiatric and gastrointestinal reactions such as: palpitations, tachycardia, hypertension, headache, tremor, tic, dyskinesia, dizziness, blurred vision, sweating, insomnia, agitation, euphoria, mania, anxiety, restlessness, nausea, diarrhea, constipation, dry mouth, and decreased appetite.
If you have questions about these drugs, consumers can call a helpline at Barr Laboratory at: 888-742-5578 between 8:00 a.m. and 8:00 p.m. EDT Monday through Friday.
—Lisa Gill, editor, Prescription Drugs
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