THYROID ALERT
- Mary Heim, RPh, FAAFM
- Sep 23
- 1 min read

Help us do something about it.
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FDA’s reclassification of Dessicated Thyroid Extract (DTE) as a biologic is unnecessary, scientifically flawed, and demonstrably harmful to patients. It strips away choice, likely increases prices, and hands control of a critical therapy to a single drugmaker.
DTE has been prescribed and used safely for more than a hundred years to treat millions of Americans with hypothyroidism. Patients depend on it when synthetic options don’t work for them.
Now, those patients will be left without a vital therapy.
We must push back against this unnecessary overreach by FDA so that patients are not collateral damage in a policy change that in effect clears the field to create a monopoly for one drugmaker.
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Tell FDA to:
Keep DTE regulated as a small-molecule drug, consistent with science and decades of precedent.
Reject a monopoly-driven reclassification that limits treatment options and drives up prices for patients.
Protect patient/provider decision-making by preserving access to DTE alongside synthetic alternatives.
The implications are serious for patients who rely on this therapy.




