Ivabradine Anpharm (ivabradine)
- Region
- 🇪🇺 EU
- Active substance
- ivabradine
- Company
- "Anpharm" Przedsiębiorstwo Farmaceutyczne S.A.
- Status
- Authorised
- Therapeutic area
- Angina Pectoris; Heart Failure
- EU approval
- Tue 08 Sep 2015
- Application
- EMEA/H/C/004187
- ATC
- C01EB17
- Official record
- www.ema.europa.eu
Indication
Symptomatic treatment of chronic stable angina pectoris Ivabradine is indicated for the symptomatic treatment of chronic stable angina pectoris in coronary artery disease adults with normal sinus rhythm and heart rate ? 70 bpm. Ivabradine is indicated: in adults unable to tolerate or with a contra-indication to the use of beta-blockers or in combination with beta-blockers in patients inadequately controlled with an optimal betablocker dose. Treatment of chronic heart failure Ivabradine is indicated in chronic heart failure NYHA II to IV class with systolic dysfunction, in patients in sinus rhythm and whose heart rate is ? 75 bpm, in combination with standard therapy including beta-blocker therapy or when beta-blocker therapy is contraindicated or not tolerated.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
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- 🇪🇺 Ivabradine JensonR Withdrawn · JensonR+ Limited
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