

A provider briefing on the Duavee shortage in 2026. Availability timeline, prescribing implications, alternatives, cost considerations, and patient access tools.
If you prescribe Duavee (conjugated estrogens 0.45 mg/bazedoxifene 20 mg) for your menopausal patients, you've likely heard from them that filling the prescription is a challenge. Duavee's availability has been inconsistent since its 2013 FDA approval, and the situation in 2026 continues to affect patient adherence and clinical decision-making.
This article provides an overview of the current supply situation, prescribing implications, cost and access considerations, and tools you can use to help your patients get the medication they need.
Duavee has faced intermittent supply constraints throughout its commercial life:
Duavee has not always appeared on the FDA Drug Shortage Database during these periods, but real-world access has been a persistent challenge.
The ongoing availability issues have several clinical implications:
Patients who cannot fill their Duavee prescriptions face gaps in therapy. For those using it for vasomotor symptom management, interruptions can mean a return of bothersome hot flashes. For those relying on it for osteoporosis prevention, gaps may compromise bone health over time.
Duavee's estrogen/SERM mechanism is distinct from traditional estrogen/progestin HRT. Bazedoxifene provides endometrial protection without the progestin-associated side effects (breast tenderness, bloating, mood changes) that some patients find intolerable. For patients who have tried and failed progestin-containing therapies, Duavee may be the preferred — or only acceptable — option.
If a patient cannot reliably access Duavee, it may be clinically appropriate to discuss alternatives proactively rather than waiting for adherence gaps. This is especially important for patients using Duavee for osteoporosis prevention, where consistent therapy is critical.
In 2026, Duavee availability varies significantly by pharmacy type and region:
Providers can direct patients to Medfinder for Providers to check real-time pharmacy stock for Duavee and other hard-to-find medications.
Duavee's cost creates an additional barrier to access:
When writing a prescription for Duavee, consider including a prior authorization letter proactively if the patient's plan requires one. Documenting that the patient has tried or is intolerant of progestin-containing alternatives can strengthen the case.
Several resources can help you and your patients navigate Duavee access:
When Duavee is unavailable or cost-prohibitive, the following alternatives may be appropriate:
For patients who specifically benefit from Duavee's SERM-based endometrial protection, there is no direct therapeutic equivalent. Document this in the chart when advocating for coverage.
For a patient-facing comparison, see: Alternatives to Duavee.
As of early 2026, no generic Duavee has been approved, and no competing estrogen/SERM combination products are in late-stage development. The availability situation is unlikely to change dramatically in the near term.
Providers can mitigate the impact by:
Duavee remains a clinically valuable option for postmenopausal women who need HRT without progestin. But its limited supply, lack of generic competition, and high cost create ongoing challenges for patients and prescribers alike.
By staying informed about the availability landscape and equipping your patients with the right tools and resources, you can help minimize treatment gaps and ensure continuity of care.
For additional resources, see our provider's guide to helping patients find Duavee and our guide on helping patients save money on Duavee.
You focus on staying healthy. We'll handle the rest.
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