Moderate Evidence Herb

Turmeric (Curcumin)

A bright yellow spice derived from the Curcuma longa plant, widely used in Ayurvedic and traditional medicine for its anti-inflammatory properties.

Updated February 20, 2026

This content is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before starting, stopping, or changing any supplement or medication regimen.

Benefits & Uses

  • Osteoarthritis symptom relief: Research suggests curcumin extracts may modestly reduce knee osteoarthritis pain and improve function compared with placebo, with some trials showing effects comparable to low-dose NSAIDs but with fewer GI complaints. Supported by multiple randomized trials and several meta-analyses (evidence: moderate).
  • Inflammation biomarkers: Meta-analyses indicate small-to-moderate reductions in CRP and some pro-inflammatory cytokines (e.g., IL-6) in various inflammatory/metabolic conditions (evidence: moderate).
  • Ulcerative colitis (adjunct): When added to standard therapy (e.g., mesalamine), curcumin may increase rates of clinical response and remission and reduce relapse risk; effects are not consistently seen in Crohn’s disease (evidence: moderate for UC; limited for Crohn’s).
  • Metabolic health: Some meta-analyses show modest improvements in glycemic control (e.g., fasting glucose, HbA1c) and lipid parameters (triglycerides, LDL-C) in type 2 diabetes/metabolic syndrome populations (effect sizes small; evidence: moderate-to-emerging).
  • Nonalcoholic fatty liver disease (NAFLD): Several RCTs suggest small improvements in liver enzymes and hepatic steatosis scores with curcumin adjunct therapy, but heterogeneity is high (evidence: emerging).
  • Depressive symptoms (adjunct): Small RCTs and pooled analyses suggest a modest reduction in depressive symptoms when used as adjunctive therapy; larger, higher-quality trials are needed (evidence: emerging).

Side Effects & Precautions

  • Common (generally mild, dose-related): Dyspepsia/acid reflux, abdominal discomfort, nausea, diarrhea, flatulence. Headache or dizziness can occur. GI effects increase with higher doses (>1 g/day of curcumin) and with piperine-enhanced products.
  • Less common: Skin rash or pruritus, yellow stool discoloration.
  • Rare but serious: Elevated liver enzymes and idiosyncratic drug-induced liver injury (hepatitis) have been reported with turmeric/curcumin supplements (including enhanced-bioavailability formulations); resolves after discontinuation in most cases. Clinically significant bleeding has occurred when combined with anticoagulants/antiplatelets. Hypoglycemia is possible when combined with glucose-lowering therapies.
  • Other considerations: Turmeric (spice) is relatively high in oxalate; high intakes may increase urinary oxalate and kidney stone risk in susceptible individuals.

Dosage & Administration

  • Curcumin extracts (standardized ~95% curcuminoids): Commonly used ranges in clinical studies are 500–2,000 mg per day, usually divided 1–3 times daily. Trials in osteoarthritis often use 500–1,500 mg/day of curcuminoids; ulcerative colitis adjunct trials commonly use 1,000–2,000 mg/day.
  • Enhanced-bioavailability formulations (e.g., curcumin-phospholipid complexes, micellar/colloidal curcumin, BCM-95, Theracurmin): Typically studied at lower nominal doses (about 200–1,000 mg/day of product), reflecting higher absorption; dosing is not interchangeable across brands.
  • Turmeric powder (root/rhizome): Trials have used roughly 1.5–6 g/day, though curcumin content is low (often 2–8%).
  • Bioavailability enhancers: Some studies combine curcumin with piperine (black pepper extract, ~5–20 mg) to increase absorption; note that piperine can also increase absorption of many drugs, raising interaction risk.
  • Administration: Often taken with meals and dietary fat to aid absorption. Optimal dosing varies by individual and condition; clinical supervision is advised for chronic use or when on medications.

Contraindications

  • Bleeding risk: Avoid or use only with medical supervision in patients with bleeding disorders or those taking anticoagulants/antiplatelets (e.g., warfarin, DOACs, clopidogrel, high-dose aspirin). Stop at least 1–2 weeks before elective surgery.
  • Gallbladder disease: Avoid in bile duct obstruction or acute biliary colic; use caution with gallstones due to choleretic effects.
  • Active peptic ulcer disease or significant GERD: May worsen GI symptoms.
  • Pregnancy and breastfeeding: Culinary amounts are generally considered safe; high-dose supplements lack robust safety data—avoid unless advised by a clinician.
  • Diabetes/hypoglycemia: Use caution with antidiabetic drugs; monitor for low blood glucose.
  • Kidney stones/hyperoxaluria: Limit high-dose turmeric powder; monitor in patients with history of calcium oxalate stones.
  • Iron-deficiency anemia: Curcumin may reduce non-heme iron absorption; separate from iron supplements and monitor ferritin/hemoglobin.
  • Liver disease or prior supplement-related liver injury: Use cautiously; consider baseline and periodic liver function tests, discontinue if enzymes rise or symptoms of hepatitis occur.

Known Interactions

Substance Type Severity Description
Warfarin caution severe Additive anticoagulant/antiplatelet effects and possible CYP2C9 inhibition may raise INR and bleeding risk.
Clopidogrel or high-dose aspirin caution moderate Additive antiplatelet effects may increase bleeding/bruising risk.
NSAIDs (e.g., ibuprofen, naproxen) caution moderate Potential additive GI irritation and bleeding risk when combined with curcumin’s antiplatelet effects.
Insulin or oral antidiabetic drugs (e.g., metformin, sulfonylureas) synergistic moderate Curcumin may modestly improve insulin sensitivity and lower glucose, potentially enhancing hypoglycemic effects; monitor blood sugar and adjust therapy as needed.
Cyclosporine or tacrolimus caution severe Curcumin may inhibit P-glycoprotein and CYP3A4, potentially increasing levels of these narrow-therapeutic-index drugs; monitor troughs closely.
Iron supplements antagonistic moderate Curcumin can chelate iron and may reduce non-heme iron absorption; separate dosing and monitor iron status if clinically relevant.
Ginkgo biloba (and other antiplatelet herbs/supplements) synergistic moderate Additive antiplatelet effects may increase bleeding risk.
Piperine (black pepper extract) synergistic moderate Enhances curcumin bioavailability substantially; may amplify both benefits and risk of drug interactions via CYP3A4/P-gp inhibition.

Check interactions with other supplements

Sources
  1. Systematic review and meta-analysis of curcumin for knee osteoarthritis symptom relief versus placebo/NSAIDs (meta-analysis) , 2016
  2. Meta-analysis of curcuminoids on systemic inflammation markers (CRP, IL-6) in randomized trials (meta-analysis) , 2016
  3. Systematic review and meta-analysis of curcumin as adjunct therapy in ulcerative colitis (induction and maintenance of remission) (meta-analysis) , 2019
  4. Meta-analysis of randomized controlled trials on curcumin and glycemic control/lipid profile in type 2 diabetes or metabolic syndrome (meta-analysis) , 2019
  5. Randomized trials of curcumin in nonalcoholic fatty liver disease showing changes in liver enzymes and steatosis indices (rct) , 2018
  6. Narrative review of turmeric/curcumin safety, pharmacokinetics, and reports of supplement-associated liver injury (review) , 2020
  7. Traditional Ayurvedic texts describing Curcuma longa for digestive and inflammatory conditions (traditional) 0

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Health Disclaimer

This content is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before starting, stopping, or changing any supplement or medication regimen.