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. 2016 Sep 28;30(6):1765–1779. doi: 10.1111/jvim.14586

Table 1.

Prohibited cardiovascular agents. Chronic administration of these agents before study entry was an exclusion criterion. Initiation of any of these agents during the study was considered an event in the time‐to‐first‐event analysis. Initiation of chronic treatment resulted in a dog being censored from the per‐protocol population

ACE Inhibitors Enalapril, benazepril, captopril, fosinopril, imidapril, lisinopril, ramipril
Angiotensin II receptor blockers Candesartan, telmisartan
Antiarrhythmic drugs Lidocaine, bretylium, flecainide, mexiletine, procainamide, phenytoin, propafenone, quinidine, tocainide, beta‐blockers [for list see below], amiodarone, sotalol, Ca++channel blockers [diltiazem, verapamil], digoxin, digitoxin
Anticholinergics Atropine, glycopyrrolate, propantheline
Beta‐blockers Atenolol, bisoprolol, carvedilol, esmolol, metoprolol, nadolol, propranolol
Diuretics Furosemide, hydrochlorothiazide, thiazides, chlorothiazide, torasemide (torsemide), spironolactone, eplerenone
Inodilators Pimobendan, levosimendan, milrinone
Phosphodiesterase V inhibitors Sildenafil, tadalafil
Positive inotropes Pimobendan, levosimendan, milrinone, isoproterenol, dobutamine, dopamine, digoxin, digitoxin
Pressor agents Epinephrine, norepinephrine, phenylephrine
Vasodilators (including nitric oxide donors) Amlodipine, hydralazine, prazosin, nitroglycerin (even topical), isosorbide di‐/mononitrate, other nitrates, nitric oxide, sodium nitroprusside, L‐arginine
Other Iloprost, epoprostenol, bosentan, known cardiac toxins, for example, doxorubicin