Heart failure is a condition where the drugs save lives and the herbs do not. This page is mostly a warning.
Heart failure is managed with four drug classes that reduce mortality — an ACE inhibitor or ARB or ARNI, a beta-blocker, a mineralocorticoid receptor antagonist, and an SGLT2 inhibitor — plus diuretics for symptoms and devices in some patients. There is no herb that reduces mortality in heart failure, and there are several that make it worse.
Hawthorn has trials in heart failure showing improvement in symptoms and exercise tolerance in some pooled analyses, and no effect on mortality. It is used in Europe as an adjunct. The concern: hawthorn has vasodilator and positive inotropic activity, and it interacts with digoxin and with antihypertensives. Combining a vasodilating herb with heart-failure medication can cause symptomatic hypotension.
Coenzyme Q10. Statins reduce CoQ10 levels by inhibiting the same mevalonate pathway. Whether that translates into statin-associated muscle symptoms is a question with mixed trial results; some trials show a reduction in muscle pain, others do not. CoQ10 is safe and is not a treatment for heart failure, though one trial in heart failure showed a mortality signal that has not been consistently replicated.
Omega-3 and other supplements: mixed evidence, discussed on the cholesterol page.
What actually matters in heart failure. Taking the four drug classes at target dose, daily weight monitoring, fluid and salt management, and reporting changes early. A person with heart failure who adds a herbal diuretic or a sodium-containing preparation can destabilise themselves quickly.
The specific interactions to avoid. Anything that raises blood pressure (liquorice), anything that lowers potassium in someone on a loop diuretic (liquorice again), anything that interferes with digoxin (hawthorn, and several herbs that affect P-glycoprotein), and anything that adds to anticoagulation if on warfarin. Ephedra and other stimulants are absolutely contraindicated.
Meta-Analysis2025Journal of nutritional science
Effects of coenzyme Q10 supplementation on myopathy in statin-treated patients: a systematic review and meta-analysis.
Supplementation of CoQ10 can reduce muscle pain in patients with SAMS, which is relevant for their well-being and treatment continuation.
PubMed 41158831 ↗
Meta-Analysis2024Cardiovascular drugs and therapy
Efficacy and Safety of Omega-3 Fatty Acids in the Prevention of Cardiovascular Disease: A Systematic Review and Meta-analysis.
Moderate evidence showed that the use of omega-3 fatty acids may reduce the risk of major cardiovascular events, myocardial infarction, and cardiovascular death.
PubMed 36103100 ↗
Meta-Analysis2023Annals of medicine
Medicine for chronic atrophic gastritis: a systematic review, meta- and network pharmacology analysis.
The results of a meta-analysis of 12 RCTs indicate that TCM intervention can improve the clinical treatment efficacy of CAG.
PubMed 38170849 ↗
Meta-Analysis2022Irish journal of medical science
Effects of coenzyme Q10 supplementation on statin-induced myopathy: a meta-analysis of randomized controlled trials.
The outcomes of this meta-analysis of existing randomized controlled trials showed that supplementation with CoQ10 did not have any significant benefit in improving statin-induced myopathy.
PubMed 33999383 ↗
Meta-Analysis2021Circulation
Effect of Long-Term Marine ɷ-3 Fatty Acids Supplementation on the Risk of Atrial Fibrillation in Randomized Controlled Trials of Cardiovascular Outcomes: A Systematic Review and Meta-Analysis.
In RCTs examining cardiovascular outcomes, marine ɷ-3 supplementation was associated with an increased risk of AF.
PubMed 34612056 ↗