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Hormone Therapy Counseling: Where Compounded BHRT Stands After FDA Restrictions

  • 74 minutes
  • 39 slides
What we'll cover
  • 0:00 Why Counseling Changed
  • 8:00 Regulatory Lines That Matter
  • 18:00 Evidence Behind Product Claims
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What you'll take away

Practical shifts you can apply this week

  • Identify Key Regulatory Changes

    Spot which FDA actions change counseling most, so visits stay current and defensible.

  • Compare Approved And Compounded Options

    Separate evidence, labeling, and quality oversight with examples patients actually ask about.

  • Evaluate Clinical Justification

    Know when compounding may fit a real gap and when preference alone is not enough.

  • Draft Clear Counseling Language

    Explain uncertainty, risk, and alternatives in plain language without sounding dismissive.

  • Design Documentation And Follow-Up

    Leave with practical charting and monitoring steps for higher-risk, preference-sensitive cases.

Agenda

What we'll cover

  1. 0:00

    Why Counseling Changed

    What shifted, why patients are asking more questions, and where this session stays practical.

  2. 8:00

    Regulatory Lines That Matter

    FDA-approved versus compounded, 503A versus 503B, and what restrictions do and do not mean.

  3. 18:00

    Evidence Behind Product Claims

    Review safety, efficacy, testing limits, and why tailored claims often outrun the data.

  4. 30:00

    Risk Translation In Visits

    Turn dose variability, contamination, and missing warnings into plain-language counseling.

  5. 40:00

    When Compounding Is Reasonable

    Use narrow, defensible criteria such as allergy, dosage-form gaps, or access disruptions.

  6. 48:00

    Scripts For Hard Conversations

    Handle natural-product requests, influencer claims, and switch discussions without friction.

  7. 55:00

    Documentation, Recap, And Q&A

    Chart rationale, monitoring, referral triggers, then close with one workflow to audit this month.

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