Open Access Articles- Top Results for Dronedarone


File:Dronedarone structure.svg
Systematic (IUPAC) name
Clinical data
Trade names Multaq
AHFS/ monograph
MedlinePlus a609034
Licence data US FDA:link
  • US: X (Contraindicated)
Pharmacokinetic data
Bioavailability 15% (with a high-fat meal)[1]
Protein binding >98%
Metabolism Extensive hepatic (mainly by CYP3A)
Half-life 13–19 hours
Excretion Feces (84%), urine (~6%)
141626-36-0 7pxN
PubChem CID 208898
ChemSpider 180996 7pxY
UNII JQZ1L091Y2 7pxY
KEGG D02537 7pxY
ChEBI CHEBI:50659 7pxY
ChEMBL CHEMBL184412 7pxY
Chemical data
Formula C31H44N2O5S
556.758 g/mol
 14pxN (what is this?)  (verify)

Dronedarone (development codename SR33589 and marketed as Multaq) is a drug by Sanofi-Aventis, mainly for the indication of cardiac arrhythmias. It was approved by the FDA on July 2, 2009. It was recommended as an alternative to amiodarone for the treatment of atrial fibrillation and atrial flutter in people whose hearts have either returned to normal rhythm or who undergo drug therapy or electric shock treatment i.e. direct current cardioversion (DCCV) to maintain normal rhythm.[2] In the United States, the FDA approved label includes a claim for reducing hospitalization, but not for reducing mortality, as a reduction in mortality was not demonstrated in the clinical development program.[3] A trial of the drug in heart failure was stopped as an interim analysis showed a possible increase in heart failure deaths, in patients with moderate to severe CHF.[4]

The U.S. label for dronedarone includes a boxed warning, stating that dronedarone is contraindicated in patients with NYHA Class IV heart failure, with NYHA Class II–III heart failure with a recent decompensation requiring hospitalization or referral to a specialized heart failure clinic, or with permanent atrial fibrillation."[1] Dronedarone is also associated with rare case of severe liver damage, including liver failure.[5]

Mechanism of action

Dronedarone has been termed a “multichannel blocker” however it is unclear which channel(s) play a pivotal role in its success.[6] Thus, dronedarone's actions at the cellular level are controversial with most studies suggesting an inhibition in multiple outward potassium currents including rapid delayed rectifier, slow delayed rectifier and ACh-activated inward rectifier.[7] It is also believed to reduce inward rapid Na current and L-type Ca channels. The reduction in K current in some studies was shown to be due to the inhibition of K-ACh channel or associated GTP-binding proteins.[6] Reduction of K+ current by 69% led to increased AP duration and increased effective refractory periods, thus shown to suppress pacemaker potential of the SA node and return patients to a normal heart rhythm.[7] In a European trial, the average time to recurrence of an arrhythmia was 41 days in the placebo group vs. 96 days in the dronedarone group (similar results obtained in the non-European trial, 59 and 158 days respectively).[8]


Chemically, dronedarone is a benzofuran derivative related to amiodarone, a popular antiarrhythmic. The use of amiodarone is limited by toxicity due its high iodine content (pulmonary fibrosis, thyroid disease) as well as by liver disease. In dronedarone, the iodine moieties are not present, reducing toxic effects on the thyroid and other organs. A methylsulfonamide group is added to reduce solubility in fats (lipophilicity) and thus reduce neurotoxic effects.[3]

Dronedarone displays amiodarone-like class III antiarrhythmic activity in vitro[9] and in clinical trials.[4] The drug also appears to exhibit activity in each of the 4 Vaughan-Williams antiarrhythmic classes.[10]




Dronedarone is less lipophilic than amiodarone, has a much smaller volume of distribution, and has an elimination half-life of 13–19 hours—this stands in contrast to amiodarone's half-life of several weeks.[1][11] As a result of these pharmacokinetic characteristics, dronedarone dosing may be less complicated than amiodarone.


  • Permanent AF (patients in whom normal sinus rhythm will not or cannot be restored)[12]
  • Recently decompensated heart failure requiring hospitalization or Class IV heart failure.[12]
  • Second-or third-degree AV block or sick sinus syndrome (except when used in conjunction with a functioning pacemaker)[12]
  • Concomitant use of a strong CYP3A inhibitor[12]
  • Concomitant use of drugs or herbal products that prolong the QT interval and may induce Torsade de Pointes[12]
  • Liver or lung toxicity related to the previous use of amiodarone[12]
  • Severe hepatic impairment[12]
  • QTc Bazett interval ≥500 ms,[12] or use with drugs or herbal supplements that prolong QT interval or increase risk of torsades de points (Class I or III antiarrhythmic agents, phenothiazines, tricyclic antidepressants, certain oral macrolides, ephedra).[citation needed]
  • Pregnancy and nursing mothers[12]
  • Hypersensitivity to dronedarone[12]
  • Hepatic impairment. In Jan 2011 the FDA advised about cases of rare, but severe, liver injury, including two cases of acute liver failure leading to liver transplant in patients treated with dronedarone (Multaq). It is not known whether routine periodic monitoring of serum liver enzymes (ALT, AST, and alkaline phosphatase) and bilirubin in patients taking dronedarone will prevent the development of severe liver injury.[5]
  • Use of cytochrome P-450 (CYP) 3a isoenzyme inhibitors (includes: clarithromycin, cyclosporine, itraconazole, ketoconazole, nefazodone, ritonavir, telithromycin, voriconazole)

Clinical trials

Clinical trials have compared dronedarone to placebo and to amiodarone, for its ability to reduce atrial fibrillation, to reduce mortality overall and from cardiac causes, and for its adverse effects, including excess mortality.[3][13] Dronedarone is a non-iodinated class III anti-arrhythmic drug which helps patients return to normal sinus rhythm. This treatment for AF is also known to reduce associated mortality and hospitalizations compared to other similar antiarrhythmic agents.[14]

In the EURIDIS and ADONIS trials in atrial fibrillation (2007), dronedarone was significantly more effective than placebo in maintaining sinus rhythm, with no difference in lung and thyroid function in the short term.[15]

However, in the ANDROMEDA study (2007), dronedarone doubled the death rate compared to placebo, and the trial was halted early.[4] ANDROMEDA enrolled patients with moderate to severe congestive heart failure, a relatively sicker patient population.

In a more recent atrial fibrillation trial, ATHENA, with 4628 subjects, dronedarone was significantly more effective than placebo in reducing the composite endpoint of first hospitalization due to cardiovascular events or death.[16] There was a significant reduction in the rate of cardiovascular death, but not in the rate of death from any cause.[3] Later post-hoc analysis of the ATHENA-results showed a significant reduction in the rate of stroke.[17]

Patients randomized to dronedarone were more likely to develop bradycardia and QT-interval prolongation (but only 1 case of Torsades). Nausea, diarrhea, rash, and creatinine elevation also were more common in the dronedarone arm.

The PALLAS trial (2011) was stopped for safety concerns due to the finding that "dronedarone increased rates of heart failure, stroke, and death from cardiovascular causes in patients with permanent atrial fibrillation who were at risk for major vascular events".[18] A Black Box warning was subsequently added by the FDA stating that the risk of death, stroke, and hospitalization for congestive heart failure doubled in patients with permanent atrial fibrillation.

Direct current cardioversion results

Dronedarone has been tested in some trials as a way to improve the success rate of electrical cardioversion. In one such trial by the Veteran's Administration it was used prepare patients for electrical conversion to sinus rhythm. In the ATHENA study, 25% of patients were started on dronedarone before cardioversion.[19] The results of a recently concluded randomized study (ELECTRA) may clarify the safety and ideal modalities of dronedarone use at the time of cardioversion.[20]

Regulatory review

Originally submitted as a New Drug Application in 2005, dronedarone was reviewed and recommended for approval on March 18, 2009 by an Advisory Committee of the United States Food and Drug Administration (FDA). The FDA is not bound by the Committee's recommendation, but it takes its advice into consideration when reviewing new drug applications.[21] The FDA approved dronedarone on July 2, 2009.

Health Canada was the second major regulatory body to approve the drug, giving its approval on August 12, 2009. The approval is for "treatment of patients with a history of, or current atrial fibrillation to reduce their risk of cardiovascular hospitalization due to this condition."[22]

The European Medicines Agency issued a Summary of Positive Opinion regarding dronedarone on 24 September 2009 recommending to the European Commission to grant a marketing authorization within the European Union.[23]


  1. ^ a b c "MULTAQ® (dronedarone) Tablets. Prescribing Information". Sanofi-Aventis U.S. LLC. March 2013. Retrieved 6 February 2014. 
  2. ^ "FDA Approves Multaq to Treat Heart Rhythm Disorder" (Press release). FDA. 2009-07-02. Retrieved July 2, 2009. 
  3. ^ a b c d Zimetbaum, PJ (2009). "Dronedarone for atrial fibrillation--an odyssey". The New England Journal of Medicine 360 (18): 1811–3. PMID 19403901. doi:10.1056/NEJMp0902248. 
  4. ^ a b c Køber L, Torp-Pedersen C, McMurray JJ et al. (June 2008). "Increased mortality after dronedarone therapy for severe heart failure". N Engl J Med 358 (25): 2678–87. PMID 18565860. doi:10.1056/NEJMoa0800456. 
  5. ^ a b "FDA Drug Safety Communication: Severe liver injury associated with the use of dronedarone (marketed as Multaq). Safety Announcement". U.S. FDA. January 14, 2011. 
  6. ^ a b Guillemare E, Marion A, Nisato D, Gautier P, “Inhibitory effects of dronedarone on muscarinic K+ current in guinea pig atrial cells,” in Journal of Cardiovascular Pharmacology, 2000 7
  7. ^ a b Aimond F, Beck L, Gautier P, Chérif OK, Davy JM, Lorente P, Nisato D, Vassort G, “Cellular and in vivo electrophysiological effects of dronedarone in normal and postmyocardial infarcted rats,” in The Journal of Pharmacology and experimental therapeutics, 2000. 11
  8. ^ Singh BN, Connolly SJ, Crijns HJ, Roy D, Kowey PR, Capucci A, Radzik D, Aliot EM, Hohnloser SH; EURIDIS and ADONIS Investigators, “Dronedarone for maintenance of sinus rhythm in atrial fibrillation or flutter,” in The New England Journal of Medicine, 2007. 12
  9. ^ Sun W, Sarma JS, Singh BN (30 November 1999). "Electrophysiological effects of dronedarone (SR33589), a noniodinated benzofuran derivative, in the rabbit heart : comparison with amiodarone". Circulation 100 (22): 2276–81. PMID 10578003. doi:10.1161/01.CIR.100.22.2276. 
  10. ^
  11. ^ Dale KM, White CM (April 2007). "Dronedarone: an amiodarone analog for the treatment of atrial fibrillation and atrial flutter". Ann Pharmacother 41 (4): 599–605. PMID 17389667. doi:10.1345/aph.1H524. 
  12. ^ a b c d e f g h i j k
  13. ^ Guillemare E, Marion A, Nisato D, Gautier P, “Inhibitory effects of dronedarone on muscarinic K+ current in guinea pig atrial cells,” in Journal of Cardiovascular Pharmacology, 2000. 7
  14. ^ Connolly SJ, Crijns HJ, Torp-Pedersen C, van Eickels M, Gaudin C, Page RL, Hohnloser SH; ATHENA Investigators, “Analysis of stroke in ATHENA: a placebo-controlled, double-blind, parallel-arm trial to assess the efficacy of dronedarone 400 mg BID for the prevention of cardiovascular hospitalization or death from any cause in patients with atrial fibrillation/atrial flutter,” in Circulation, 2009.8
  15. ^ Singh BN, Connolly SJ, Crijns HJ et al. (September 2007). "Dronedarone for maintenance of sinus rhythm in atrial fibrillation or flutter". N Engl J Med 357 (10): 987–999. PMID 17804843. doi:10.1056/NEJMoa054686. 
  16. ^ Hohnloser SH, Crijns HJ, van Eickels M et al. (February 2009). "Effect of Dronedarone on Cardiovascular Events in Atrial Fibrillation". N Engl J Med 360 (7): 668–678. PMID 19213680. doi:10.1056/NEJMoa0803778. 
  17. ^ Connolly SJ, Crijns HJGM, Torp-Pedersen C, van Eyckels M, Gaudin C, Page RL, Hohnloser SH (September 2009). "Analysis of Stroke in ATHENA: A Placebo-Controlled, Double-Blind, Parallel-Arm Trial to Assess the Efficacy of Dronedarone 400 mg BID for the Prevention of Cardiovascular Hospitalization or Death From Any Cause in Patients With Atrial Fibrillation/Atrial Flutter". Circulation 120 (13): 1174–80. PMID 19752319. doi:10.1161/CIRCULATIONAHA.109.875252. 
  18. ^ Connolly SJ, Camm AJ, Halperin JL et al. (December 2011). "Dronedarone in High-Risk Permanent Atrial Fibrillation". N Engl J Med 365 (24): 2268–2276. doi:10.1056/NEJMoa1109867. 
  19. ^ Effect of Dronedarone on Cardiovascular Events in Atrial Fibrillation.Stefan H. Hohnloser, M.D., Harry J.G.M. Crijns, M.D., Martin van Eickels, M.D., Christophe Gaudin, M.D., Richard L. Page, M.D., Christian Torp-Pedersen, M.D., and Stuart J. Connolly, M.D. for the ATHENA Investigators. N Engl J Med 2009; 360:668-678February 12, 2009DOI: 10.1056/NEJMoa0803778
  20. ^
  21. ^ FDA briefing document on dronedarone
  22. ^
  23. ^ Summary of Positive Opinion (retrieved 1 December 2009)