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1 conazole, voriconazole, or posaconazole; and dronedarone.
2 e among patients who received treatment with dronedarone.
3 and liver disease among patients exposed to dronedarone.
4 to investigate the inactivation of CYP450 by dronedarone.
5 regarding clinical efficacy of azimilide and dronedarone.
6 goxin, there were 6 cardiovascular deaths on dronedarone (1.7%/year) and 8 on placebo (2.2%/year; adj
10 We identified 4 placebo-controlled trials of dronedarone, 4 placebo-controlled trials of amiodarone,
11 Parallel Arm Trial to Assess the Efficacy of Dronedarone 400 mg bid for the Prevention of Cardiovascu
13 d to placebo, ranolazine alone (750 mg BID), dronedarone alone (225 mg BID), or one of the combinatio
14 ntration on day 7 was 1.1 (0.7,1.5) ng/mL on dronedarone and 0.7 (0.5,1.1) ng/mL on placebo (P<0.001)
15 In PALLAS, 1619 patients were randomized to dronedarone and 1617 to placebo, of whom 544 (33.6%) and
16 were 15 (8.6%/year) cardiovascular deaths on dronedarone and 2 (1.2%/year) on placebo (adjusted hazar
17 n digoxin, there were 2 arrhythmic deaths on dronedarone and 4 on placebo (P value for interaction 0.
18 on are 2.19 microM and 0.0056 minute(-1) for dronedarone and 5.45 microM and 0.056 minute(-1) for NDB
19 We demonstrated for the first time that both dronedarone and its main metabolite N-desbutyl dronedaro
23 digoxin, there were 11 arrhythmic deaths on dronedarone and none on placebo; and in patients not on
25 aluate the effectiveness of a combination of dronedarone and ranolazine in suppression of atrial fibr
26 that raise questions regarding the safety of dronedarone and several new promising techniques in AF a
28 croM and 0.039 minute(-1), respectively, for dronedarone, and 6.24 microM and 0.099 minute(-1), respe
29 summarize the available evidence concerning dronedarone, and offer practical recommendations to heal
30 for the inactivation of CYP3A4 and CYP3A5 by dronedarone are 51.1 and 32.2, and the partition ratios
32 ctive investigation, including azimilide and dronedarone, are compounds with multiple electrophysiolo
35 The present analysis examines whether the dronedarone-digoxin interaction might explain these adve
36 olazine (750 mg BID) combined with 2 reduced dronedarone doses (150 mg BID and 225 mg BID; chosen to
37 There has been concern about the safety of dronedarone, especially for patients with heart failure
38 oup and 102.3+/-24.7 beats per minute in the dronedarone group (P<0.001); the corresponding rates in
41 ustment for cofactors, patients who received dronedarone had lower mortality than other AF patients (
44 e that the available data support the use of dronedarone in select patient populations as a second- o
46 of the underlying mechanisms associated with dronedarone-induced hepatotoxicity and clinical drug-dru
47 in-house preliminary study demonstrated that dronedarone inhibits cytochrome P450 (CYP) 3A4 and 3A5 i
56 onedarone and its main metabolite N-desbutyl dronedarone (NDBD) inactivate CYP3A4 and CYP3A5 in a tim
57 ible metabolite-intermediate complex between dronedarone/NDBD and CYP3A4/CYP3A5, partial recovery of
58 current digoxin use on the adverse effect of dronedarone on cardiovascular death, but not on occurren
60 nent Atrial Fibrillation Outcome Study Using Dronedarone On Top Of Standard Therapy Trial (PALLAS), d
61 clinical trials have evaluated the impact of dronedarone on various cardiovascular end points and yie
64 trial evidence found amiodarone superior to dronedarone (OR: 0.49; 95% CI: 0.37 to 0.63; p < 0.001)
65 drug discontinuation with amiodarone versus dronedarone (OR: 1.81; 95% CI: 1.33 to 2.46; p < 0.001).
66 first AAD prescription (amiodarone, sotalol, dronedarone, or Class Ic) within 14 days post-first AF e
71 (150 mg BID and 225 mg BID; chosen to reduce dronedarone's negative inotropic effect-see text below)
74 risk of AF hospitalization was greater with dronedarone than Class Ic (hazard ratio [HR] 1.59; 95% c
75 sought to compare the efficacy and safety of dronedarone versus amiodarone for the prevention of recu
78 fidence interval [CI]: 0.08 to 0.19) but not dronedarone versus placebo (OR: 0.79; 95% CI: 0.33 to 1.
79 l mortality rate among patients who received dronedarone was 1.3% compared with 14.0% in the control
80 e On Top Of Standard Therapy Trial (PALLAS), dronedarone was associated with both increased cardiovas
84 y moderate dose ranolazine plus reduced dose dronedarone, with good tolerance/safety, in the populati
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