Interaction Guide · Research summary

Can I take Camellia Sinensis Leaf Extract with Gefitinib?

Review Camellia Sinensis Leaf Extract with Gefitinib: possible adverse effects, preparation details, evidence limits, and sources.

Prepared by Dr. Edward M.Kim, PharmD · Clinical Director, SupplementSafety editorial team

Research summary published · Prepared · Editorial update

The short answer

Have green tea extract reviewed before taking it with gefitinib. Concentrated extracts have caused liver-enzyme elevations in a human trial, but a change in gefitinib absorption or effectiveness has not been established.

What this answer covers

Concentrated Camellia sinensis leaf extracts with oral gefitinib; EGCG dose, duration and formulation distinguished from brewed tea.

Supplement or preparation
Camellia Sinensis Leaf Extract
Medication ingredient
gefitinib

Check the exact treatment

This review concerns oral gefitinib tablets used for selected EGFR-mutated lung cancers. The prescribed tablet and dosing plan matter. Follow the cancer team’s instructions; food, acid reducers and supplements should be reviewed together.

The liver signal concerns concentrated extract

In a year-long placebo-controlled study, an extract supplying 843 mg EGCG daily caused more ALT elevations than placebo. Overall adverse-event and serious-event frequencies were not significantly different. The participants were postmenopausal women, not patients receiving gefitinib, so this cannot quantify a combined risk.

An enzyme theory is not a measured drug interaction

A small two-week study of a decaffeinated green tea extract found no significant changes in CYP3A4 or CYP2D6 probe-drug measures. It did not test gefitinib or prove long-term liver safety. Laboratory cancer-cell findings also cannot establish improved or reduced gefitinib effectiveness in people.

Bring the extract label to the team

Report the EGCG amount, dose and other ingredients, and follow gefitinib’s liver-testing plan. Do not use the extract to boost cancer treatment or assume a time gap prevents liver injury. Promptly report yellowing skin or eyes, dark urine or persistent loss of appetite.

Evidence and practical considerations

Side effects & toxicity

A conditional liver-risk precaution is supported; the vague claim of changed gefitinib effectiveness is not supported by the checked human evidence.

Exact scope
Concentrated Camellia sinensis leaf extracts with oral gefitinib; EGCG dose, duration and formulation distinguished from brewed tea. with RxNorm 328134 IN gefitinib. Current exact oral product: Gefitinib oral tablets. Salt/formulation named explicitly; no transfer to unrelated drugs or routes.
Medication form and route
Oral

What remains uncertain

  • No exact gefitinib-extract clinical trial or PK measurement. Separate liver signal and CYP-probe null findings retained; product mass is not EGCG dose.

Factors that may matter: Exact oral formulation and supplement preparation; Drug exposure versus clinical outcomes; Dose, duration and other medicines; Individual monitoring plan.

Research conclusion: supported with conditions · Evidence assessment: moderate

Read the supporting source summaries

Source 1: Current original prescribing information

dailymed.nlm.nih.gov · Source check Sep 10, 2026

Population: Patients prescribed the exact oral formulation.

Six-hour antacid separation; CYP3A induction can lower exposure; periodic liver monitoring.

How this applies: RxNorm 328134 IN gefitinib. Current exact oral product: Gefitinib oral tablets. Salt/formulation named explicitly; no transfer to unrelated drugs or routes.

Exact current oral product source, not a clinical trial of every supplement. Formulation, dose, population and mechanism remain explicit.

Source 2: Original clinical research

pubmed.ncbi.nlm.nih.gov · Source check Sep 10, 2026

Population: 1075 postmenopausal women randomized.

ALT elevations 6.7% versus 0.7%; overall adverse and serious adverse event frequencies not significantly different.

How this applies: Exact reported preparation, population and endpoints; transfer to gefitinib explicitly limited.

Abstract-only; original body challenge retained. Not gefitinib co-use, every extract or brewed tea. Biomarker injury signal does not measure combined liver failure risk.

Source 3: Original clinical research

pubmed.ncbi.nlm.nih.gov · Source check Sep 10, 2026

Population: 11 healthy volunteers.

No significant CYP3A4/2D6 probe changes.

How this applies: Exact reported preparation, population and endpoints; transfer to gefitinib explicitly limited.

Abstract-only small short probe study, not gefitinib exposure or long-term liver safety.

Source 4: Medication terminology

rxnav.nlm.nih.gov · Source check Sep 10, 2026

Population: Terminology.

gefitinib is IN.

How this applies: Exact ingredient.

Not clinical evidence.

Research assessment: · Open full citations ↗

Review and change history

Publication status
Published research summary
Clinical review
Not yet recorded
DateUpdate
Research summary published
Article prepared
Sources checked and article drafted.

Article revision: 572055c8b2664e99

This guide brings together the evidence records used by our interaction checker. Each finding retains its own preparation limits, research date, and source summaries.

Full citations require verification. Reading this answer and the source summaries does not.

Taking other supplements or medications?

Use the checker to explore your other combinations. Ask a pharmacist to review the exact products, amounts and medical conditions in your complete list.

Open the interaction checker

Information, not medical advice. Do not change prescribed treatment based on this guide.