Critical Pharmacodynamic Warning

pomalidomide weakly inhibits the 1A2 metabolic pathway.

When patients take pomalidomide concurrently with drugs metabolized by 1A2, the risk of adverse effects may significantly increase. This interaction affects drug clearance and systemic exposure, potentially leading to toxicity or reduced therapeutic efficacy.

Clinical Impact: As a weak inhibitor, pomalidomide can alter the metabolism of substrate drugs, requiring careful monitoring and potential dose adjustments.

Clinical Overview for pomalidomide

This page outlines known interaction pathways involving pomalidomide, focusing primarily on its profile as a Weak inhibitor affecting the 1A2 pathway.

Enzyme Interaction Profile

pomalidomide demonstrates weak inhibitor potency against 1A2. This level of inhibition causes ≥1.25-fold but <2-fold increase in AUC of substrate drugs.

Inhibitor

A substance that slows down or prevents an enzyme from metabolizing a drug. Inhibitors can lead to increased drug concentrations in the body, potentially causing toxicity or enhanced therapeutic effects.

Clinical Example: pomalidomide weakly inhibits 1A2

Inducer

A substance that speeds up enzyme activity, causing drugs to be cleared from the body faster. Inducers can reduce drug effectiveness by lowering concentrations below therapeutic levels.

Known Inducers: broccoli
Interaction Details
Drug Name pomalidomide
Affected Enzyme 1A2
Inhibitor Strength Weak inhibitor Low Severity
Inducers broccoli
Inhibitors cimetidine
Clinical Recommendations

Generally safe for co-administration. Routine monitoring recommended.

Monitoring Parameters:
  • Therapeutic drug levels
  • Adverse effect monitoring
  • Clinical response assessment
Dose Considerations:
  • Consider dose reduction
  • Evaluate alternative therapies
  • Adjust based on response
Quick Facts
Interaction ID
1634
Primary Pathway
1A2
Interaction Type
Enzyme Inhibition
Clinical Phase
Low Severity
Clinical Significance

Minor clinical significance. Routine monitoring sufficient.

Information Sources
  • FDA Drug Interaction Database
  • Clinical Pharmacology Guidelines
  • Pharmaceutical Labeling Information
  • Published Clinical Studies
Last updated: June 16, 2026
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