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. 2020 Jul 15;35(2):249–259. doi: 10.1007/s10557-020-07037-2

Table 1.

Common drug–drug interactions and recommendations for use in patients with COVID-19

Class of drug Concerns Recommendation
Antiplatelets P2Y12 inhibitors Increased risk of bleeding With fibrinolytics and patients with coagulopathy: clopidogrel is preferred
In patients receiving lopinavir/ritonavir, increased risk of bleeding with ticagrelor, and decreases antiplatelet activity with clopidogrel Prasugrel is recommended with lopinavir/ritonavir
Glycoprotein IIb/IIIa Inhibitors Increased risk of bleeding

Their use should be restricted

Can be considered if needed

Abciximab is not recommended

Anticoagulants LMWH Increased risk of bleeding

In patents with coagulopathy and with fibrinolytic therapy, LMWH is preferred

(If angiography is going to be done within 24 h after fibrinolytic therapy, UFH is still the best option)

UFH Increased risk of bleeding If the patient is considered to be at high bleeding risk, UFH could be considered.
Rivaroxaban

In patients receiving lopinavir/ritonavir, increased risk of bleeding

Interaction with tocilizumab

Contraindicated with lopinavir/ritonavir

Not recommended with tocilizumab

Apixaban

In patients receiving lopinavir/ritonavir, increased risk of bleeding

Interaction with tocilizumab

Contraindicated/reduce dose by 50% with lopinavir/ritonavir

Not recommended with Tocilizumab

Dabigatran In patients receiving lopinavir/ritonavir, increased risk of bleeding Use not recommended/suggested as an option, data lacking
Edoxaban In patients receiving lopinavir/ritonavir, increased risk of bleeding

Stroke prevention in non-valvular AF: no dose adjustment

VTE indication: reduce dose by 50%

Warfarin In patients receiving lopinavir/ritonavir/tocilizumab, may reduce or increase INR OAC of choice, monitor INR
Fibrinolytics Increased risk of bleeding Tenecteplase is preferred
Statins Increased risk of hepatotoxicity Monitor LFT

Increased effect with lopinavir/ritonavir

Decreased effect with tocilizumab

Reduce dose with lopinavir/ritonavir

Monitor with tocilizumab

Beta-blockers Increased risk of bradycardia, hypotension and AV block with concomitant use of protease inhibitors

Metoprolol and bisoprolol are preferred

Monitor BP and HR

ACEI/ARB/ARNI Decreased effects of losartan and irbesartan with lopinavir/ritonavir

Continuation of ACEI/ARB

Monitor BP, SCr, and K

Increased effects of valsartan with lopinavir/ritonavir
Increased concentration of sacubitril with lopinavir/ritonavir
Mineralocorticoid antagonists Increased risk of adverse effect with lopinavir/ritonavir

Spironolactone is preferred

Eplerenone is contraindicated

Monitor serum electrolytes and SCr

Diuretics Increase the concentration of indapamide with lopinavir/ritonavir

Monitor BP, serum electrolytes for prevention of TdP

Monitor BUN/SCr

Digoxin Increased risk of toxicity Monitor digoxin concentration
Ivabradine Increased risk of adverse effect with lopinavir/ritonavir Do not co-administer with lopinavir/ritonavir
Antiarrhythmics Increased risk of QT prolongation and TdP with concomitant use of chloroquine/hydroxychloroquine

Monitor ECG before initiation

Maintain serum Mg > 2 and K > 4 mg/dL

Increased antiarrhythmic effects with protease inhibitors

Lidocaine and quinidine are preferred. Monitor ECG and adjust dose if necessary

Flecainide and propafenone are not recommended

ECG, BP, LFT, and TFT should be monitored periodically with reduced dose of amiodarone

ACEI: angiotensin converting enzyme inhibitor; ARB: angiotensin receptor blocker; ARNI: angiotensin receptor neprilysin inhibitor; AF: atrial fibrillation; AV: atrioventricular; BP: blood pressure; BUN: blood urea nitrogen; ECG: electrocardiogram; HR: heart rate; INR: international normalized ratio; LFT: liver function test; LMWH: low molecular weight heparin; OAC: oral anticoagulant; SCr: serum creatinine; TdP: torsade de pointes; TFT: thyroid function test; UFH: unfractionated heparin; VTE: venous thromboembolism