Interaction Guide · Research summary

Can I take Commiphora Wightii with Diltiazem?

Review Commiphora Wightii with Diltiazem: absorption and effectiveness, 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

A small study found lower diltiazem exposure with gugulipid. Discuss the exact guggul product before use, but do not rely on an eight-hour gap: the study measured blood samples for eight hours and did not test that spacing.

What this answer covers

Oral diltiazem with gugulipid, an extract linked in NLM terminology to Commiphora wightii/C.mukul. Evidence does not authenticate every whole-plant or resin product.

Supplement or preparation
Commiphora wightii
Medication ingredient
diltiazem

What the original study found

Seven healthy men received a single 60 mg oral diltiazem dose with or without 1 g gugulipid in a crossover study. Peak concentrations and exposure measured through eight hours fell significantly. The study did not measure loss of angina or BP control in patients.

Eight hours was the measurement window

Blood was sampled hourly for up to eight hours. That is not evidence that taking the supplement eight hours before or after diltiazem prevents the effect. The study also does not define a dose adjustment for extended-release diltiazem.

Match the studied extract

NLM’s substance record links gugulipid with Commiphora wightii extract and C.mukul extract. The historical study abstract gives limited product characterization. Whole-plant powders, different resin extracts and combination products cannot be assumed to deliver the same exposure.

Discuss use before changing therapy

Show the prescriber or pharmacist the extract strength and daily dose. They can decide whether to avoid the product or monitor treatment response. Do not increase diltiazem or stop it yourself. Report worsening BP control or angina promptly and follow your existing plan for chest pain.

Evidence and practical considerations

Absorption & effectiveness

Single-dose gugulipid reduced early diltiazem exposure in seven healthy men; this supports a preparation-limited concern, not a validated eight-hour dosing rule.

Exact scope
Oral diltiazem with gugulipid, an extract linked in NLM terminology to Commiphora wightii/C.mukul. Evidence does not authenticate every whole-plant or resin product. with Current RxNorm confirms diltiazem RxCUI 3443 IN. Oral hydrochloride once-daily capsules; immediate-release single-dose originals explicitly distinguished. No transfer to topical fissure treatment or IV administration.
Medication form and route
Oral

What remains uncertain

  • Abstract-only seven-person single-dose trial, early AUC and incompletely described extract. No validated eight-hour gap, ER equivalence or clinical failure outcome.

Factors that may matter: Exact preparation and dose; Oral formulation; Blood pressure and pulse; Other medicines.

Research conclusion: supported with conditions · Evidence assessment: low

Read the supporting source summaries

Source 1: Current prescribing information

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

Population: Patients prescribed diltiazem hydrochloride extended-release capsules.

Avoid known CYP3A4 inducers: rifampin lowered concentrations to undetectable. Bradycardia, conduction and hypotension warnings apply.

How this applies: Exact ingredient through the stated labeled salt and oral formulation. Current RxNorm confirms diltiazem RxCUI 3443 IN. Oral hydrochloride once-daily capsules; immediate-release single-dose originals explicitly distinguished. No transfer to topical fissure treatment or IV administration.

Other-drug inducer magnitudes not transferred. Guggul eight-hour sampling is not spacing; small conflicting grapefruit juice studies retained.

Source 2: Original clinical research

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

Population: Seven healthy men in the diltiazem arm of a randomized crossover.

Peak concentration and AUC measured through eight hours were significantly reduced.

How this applies: Exact preparation and endpoint boundaries retained; this is not a measured diltiazem combination unless explicitly stated.

Abstract-only; no clinical disease-control outcomes, no tested eight-hour separation, limited extract characterization and no ER combination trial.

Source 3: Substance identity record

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

Population: Substance terminology.

Identifies the extract terminology bridge used for the original study.

How this applies: Explicit extract-only bridge.

Does not authenticate the historical study batch or prove every whole-plant product equivalent. Browser HTML was an access-denied page; successful API JSON is the actual identity source.

Source 4: Medication terminology

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

Population: Terminology.

diltiazem 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
Article prepared
Sources checked and article drafted.
Research summary published

Article revision: 9e59a2f8e13963f9

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.

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