PROGRAM APPLICATION - radiuspharm.com
PROGRAM APPLICATION PATIENT ELIGIBILITY CRITERIA: Medicare Beneficiary Commercially-Insured but Not Covered Uninsured •Patient must have an FDA-approved, on-label diagnosis for TYMLOS® (abaloparatide) injection To avoid return of an incomplete application, complete all fields
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Reference ID: 4090621 - Home - Radius
radiuspharm.comTYMLOS may cause hypercalcemia. TYMLOS is not recommended in patients with pre-existing hypercalcemia or in patients who have an underlying hypercalcemic disorder, such as
HIGHLIGHTS OF PRESCRIBING INFORMATION …
radiuspharm.comIn this study, the incidence of all-cause mortality was 0.4% in the TYMLOS group and 0.6% in the placebo group. The incidence of serious adverse events was 10% in the TYMLOS group and 11% in the placebo group. The percentage of patients who discontinued study drug due to adverse events was 10% in the TYMLOS group and 6% in the placebo group.
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