Free Newsletter
Feds to study ADHD drugs for heart risks
Do they or don't they? The feds aim to find out whether drugs for attention deficit hyperactivity disorder actually increase the risk of heart problems. The FDA and the Agency for Healthcare Research and Quality will review clinical data on 500,000 patients who took ADHD meds over a seven-year period ending in 2005, looking for any patterns that indicate the patients also developed high blood pressure or other cardiovascular problems.
This new study stems from concerns raised at an FDA advisory committee meeting last year, when the panel recommended stronger warnings for the drugs because of potential cardiac risks. The FDA then began its own research, but budgetary constraints threatened its completion. Americans spent about $1.5 billion last year on the three top ADHD drugs: Concerta (Johnson & Johnson), Strattera (Eli Lilly), and Adderall (Shire).
- read the statement from the FDA
- check out this Los Angeles Times article
Related Articles:
FDA committee votes against ADHD "black box." Report
FDA panel wants 'black box' on ADHD drugs. Report
FDA committee to review ADHD risks. Report
Comments
Post new comment
Paid Research Reports
- Stakeholder Opinions: Vaccines in Emerging Markets (Asia) - Opportunities in China, India, South Korea and Taiwan
- Big Pharma Performance Before, During and Beyond the Global Recession
- Optimizing Lifecycle Management: Maximizing commercial lifespan through label expansion and combination products
- The CRO Market Outlook: Emerging markets, leading players and future trends
- Pharmaceutical Sales Force Effectiveness Strategies
- Commercial Insight: Influenza Vaccines and Antivirals - The pandemic's long-term impact





