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

Table A2.

Interacting drugs prescribed to cases and controls on direct oral anticoagulant therapy in a 30‐day time window prior to the index date

Cases (n = 393) Controls (n = 1494)
n (%) n (%)
Concomitant use of at least 1 drug with PK interaction 177 (45.0) 765 (51.2)
Strong CYP3A4 and/or P‐gp inhibitor comedication
Ketoconazole 0 0
Cyclosporine 0 0
Itraconazole 0 1
Dronedarone <5 <5
Tacrolimus 0 0
Moderate CYP3A4 and/or P‐gp inhibitors
Amiodarone 7 (1.8) 40 (2.7)
Posaconazole 0 0
Quinidine 0 0
Verapamil 5 (1.3) 12 (0.8)
Digoxin 54 (13.7) 192 (12.9)
Diltiazem 7 (1.8) 69 (4.6)
Simvastatin 76 (19.3) 374 (25.0)
Atorvastatin 59 (15.0) 232 (15.5)
Ticagrelor <5 0
Fluconazole <5 <5
Clarithromycin <5 7 (0.5)
Erythromycin <5 <5
Concomitant use of at least 1 drug with PD interaction 85 (21.6) 202 (13.5)
Antiplatelets 41 (10.4) 90 (6.0)
Ticlopidine <5 0
Clopidogrel 13 (3.3) 27 (1.8)
Low‐dose acetylsalicylic acid 32 (8.1) 66 (4.4)
NSAIDs 7 (1.8) 19 (1.3)
Diclofenac 0 0
Naproxen <5 5 (0.3)
SSRIs * 41 (10.4) 95 (6.4)
SNRI 6 (1.5) 16 (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.

All the cases <5 are according to the regulations of ISAC for CPRD database.