Quercetin for Health & Longevity

Created on 10/30/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5.5 – Audit

Quercetin, a plant pigment in onions, apples and tea, is an inexpensive dietary supplement studied for blood pressure, infection and aging. The most consistent finding is a small blood-pressure drop, mainly when pressure is already raised. Pairing it with a prescription cancer drug to clear worn-out cells remains unproven. Alone at usual doses, it appears well tolerated for up to three months; its main risk is interactions with common drugs. (Full Review)

Protocol

Daily cardiometabolic dose
500–730 mg/day
500 mg once or twice daily typical; 1,000 mg/day commonly split into two 500 mg doses
Time of day
With a fat-containing meal
Roughly doubles absorption; morning dosing during senolytic courses
Intermittent senolytic dose
Dasatinib 100 mg plus quercetin 1,000–1,250 mg
On 2–3 consecutive days, weekly for 3 weeks or every 28 days
Time to effect
Blood pressure
Within 2–4 weeks
Largest with elevated pressure
Uric acid
Within 2–4 weeks
Fell from a high-normal baseline
Liver fat
After 12 weeks
In fatty liver disease

Benefits

Contraindications
  • Pregnancy and breastfeeding
  • Chronic kidney disease
  • Estrogen-dependent cancers (e.g., hormone-receptor-positive breast cancer)
  • People receiving chemotherapy
  • People on warfarin or narrow-therapeutic-index transporter substrates (e.g., digoxin, cyclosporine) without monitoring
Key Interactions
  • P-glycoprotein substrates (fexofenadine): exposure rose
  • Statins carried by OATP1B1 (pravastatin): exposure rose
  • CYP2C9 substrates (diclofenac; also celecoxib): diclofenac exposure rose
  • CYP3A substrates (midazolam; by extension nirmatrelvir in Paxlovid, tacrolimus): midazolam exposure fell
  • CYP2E1 and CYP1A2 substrates (chlorzoxazone; caffeine; theophylline): chlorzoxazone exposure rose, caffeine metabolism slowed
Theoretical (inferred from mechanism)
  • Antihypertensive drugs (such as amlodipine, lisinopril, losartan): possible dizziness or low blood pressure
  • Digoxin: levels could rise
  • Chemotherapy drugs that act through oxidative damage (e.g., doxorubicin, cisplatin): may interfere
  • Dasatinib in senolytic stacks: dasatinib exposure could change
  • Blood-pressure-lowering supplements (fish oil, garlic, magnesium): possible dizziness or low blood pressure
  • Antiplatelet supplements (fish oil, ginkgo, vitamin E): bleeding risk
  • Iron supplements: lower iron uptake
  • Alcohol: possible headache and flushing

Risk & Side Effects

  • High:
  • Medium: Altered blood levels of co-administered drugs
  • Low: Mild gastrointestinal discomfort and other minor effects; kidney injury at high exposure; adverse events of senolytic regimens with dasatinib
  • Speculative: Tumor promotion in rodent models; bleeding tendency; reduced thyroid function; reduced iron absorption; headache with alcohol; demyelination with dasatinib

Monitoring

Marker Target Why
Blood pressure <120/<80 mmHg Primary benefit marker
Serum uric acid 3.5–7.2 mg/dL men, 2.6–6.0 mg/dL women Expected to change
Serum creatinine with eGFR 0.7–1.3 mg/dL men, 0.6–1.1 mg/dL women Safety check: a sustained rise stops use
ALT ≤29–33 U/L men, ≤19–25 U/L women Safety check; also expected to fall in fatty liver
INR (only if on warfarin) No established target for quercetin; change from own baseline within the prescriber's range Safety check: a rise signals an interaction

Cadence: Baseline before starting; home blood pressure weekly for the first 4 weeks, then monthly; uric acid, creatinine and ALT at 8–12 weeks, then every 6–12 months; INR 3–7 days after starting or stopping quercetin while on warfarin

Qualitative Assessment

  • Stomach comfort and headache frequency
  • Sleep quality, especially during senolytic courses
  • Muscle soreness and recovery after hard training
  • Frequency and duration of upper respiratory infections
  • Energy and fatigue levels
  • Unusual bruising or bleeding