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. 2020 Feb 21;86(6):1150–1164. doi: 10.1111/bcp.14227

Table A4.

Interacting drugs prescribed to cases and controls on direct oral anticoagulant therapy in a 60‐day time window prior to the index date

Cases (n = 393) Controls (n = 1494)
Concomitant use of n (%) n (%)
Concomitant use of at least 1 drug with PK interaction 224 (57.0) 936 (62.7)
Strong CYP3A4 and/or P‐gp inhibitor comedication
Ketoconazole, 0 0
Cyclosporine 0 0
Itraconazole 0 <5
Dronedarone <5* <5
Tacrolimus 0 0
Moderate CYP3A4 and/or P‐gp inhibitors
Amiodarone 10 (2.5) 51 (3.4)
Posaconazole 0 0
Quinidine 0 0
Verapamil 5 (1.3) 18 (1.2)
Digoxin 65 (16.5) 228 (15.3)
Diltiazem 11 (2.8) 82 (5.5)
Simvastatin 95 (24.2) 467 (31.3)
Atorvastatin 76 (19.3) 294 (19.7)
Ticagrelor <5 <5
Fluconazole 0 0
Clarithromycin 0 0
Erythromycin <5 9 (0.6)
Concomitant use at least 1 drug with PD interaction 123 (31.3) 278 (18.6)
Antiplatelets 70 (17.8) 146 (9.8)
Ticlopidine 0 0
Clopidogrel 23 (5.9) 40 (2.7)
Acetylsalicylic acid 55 (14.0) 110 (7.4)
NSAIDs 9 (2.3) 29 (1.9)
Diclofenac <5 <5
Naproxen 5 (1.3) 11 (0.7)
SSRIs * 53 (13.5) 113 (7.6)
SNRI 8 (2.0) 17 (1.1)
Enzyme inducers
Rifampicin 0 0
Carbamazepine <5 <5
Phenytoin <5 <5
Other inducers 0 0

PK, pharmacokinetic; PD, pharmacodynamic; ACE, angiotensin‐converting‐enzyme; NSAIDs, nonsteroidal anti‐inflammatory drug; SSRIs, Selective serotonin reuptake inhibitor; SNRIs, Serotonin–norepinephrine reuptake inhibitor.

*

The SSRIs we assessed were fluoxetine, paroxetine, sertraline, citalopram, escitalopram, sertraline, and nefazodone. The SNRIs we assessed were venlafaxine and duloxetine.

**

According to CPRD policy, all cells having less than 5 patients are shown as “<5”.