Shire Presents Data on Efficacy of Mydayis, Unmet Need for Adults With ADHD
Mydayis’ debut this weekend at the 30th US Psychiatric and Mental Health Congress in New Orleans, Louisiana, came after more than a decade of studies for the treatment for attention deficit hyperactivity disorder (ADHD). During the meeting, Shire PLC presented consolidated data involving adults aged 18 to 55 years; in June, FDA approved the drug for patients as young as 13. The drug has the same active ingredient as Adderall XR, but works up to 16 hours through a 3-bead technology that releases amphetamine in the stomach and at points in the small intestine over several hours.
Other Articles in this Edition
ADHD Kids Can Be Still – If They’re Not Straining Their Brains
The Role Developmental Motor Skills Play in Your Child’s ADHD
FDA Clears Liquid Extended-Release Amphetamine for ADHD
Adult ADHD Patients Want Longer Acting Medications
Shire Presents Data on Efficacy of Mydayis, Unmet Need for Adults With ADHD
Top ADHD Myths and How Adults Can Overcome Them
Why people with ADHD can be successful in business
Duke receives $12.5 million grant to study children with both ADHD and autism
Things Parents Of Children With ADHD Wish Someone Had Told Them