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Abaloparatide

    DEA Class; Rx

    Common Brand Names; Tymlos

    • Parathyroid Hormone Analogs

    An analog of human parathyroid hormone related peptide [PTHrP(1-34)]
    Used for the treatment of postmenopausal women with osteoporosis at high risk for fracture
    Cumulative use for more than 2 years during a patient’s lifetime is not recommended

    Women

    • Indicated for treatment of osteoporosis in postmenopausal women at high risk for fracture (defined as history of osteoporotic fracture, multiple risk factors for fracture), or patients who have failed or are intolerant to other available osteoporosis therapy

    • Shown to reduce risk of vertebral and nonvertebral fractures in postmenopausal women with osteoporosis

    Men

    • Indicated to increase bone density in men with osteoporosis at high risk for fracture (defined as history of osteoporotic fracture or multiple risk factors for fracture), or patients who have failed or are intolerant to other available osteoporosis therapy

    History of systemic hypersensitivity to drug or components of product formulation

    Women

    • Injection site redness (58%)

    • Hypercalciuria (11%)

    • Injection site edema (11%)

    • Dizziness (10%)

    • Nausea (8%)

    • Headache (8%)

    • Palpitations (5%)

    • Orthostatic hypotension (4%)

    • Fatigue (3%)

    • Upper abdominal pain (3%)

    • Hypercalcemia (3%)

    • Vertigo (2%)

    • Tachycardia (2%)

    Men

    • Injection site erythema (13%)

    • Dizziness (9%)

    • Arthralgia (7%)

    • Injection site swelling (7%)

    • Increased serum uric acid (7%)

    • Injection site pain (6%)

    • Orthostatic hypotension (6%)

    • Contusion (3%)

    • Abdominal distention (3%)

    • Diarrhea (3%)

    • Nausea (3%)

    • Hypercalcemia (3%)

    • Abdominal pain (2%)

    • Bone pain (2%)

    • Urolithiases (2%)

    May cause orthostatic hypotension, typically within 4 hr after injection; associated symptoms may include dizziness, palpitations, tachycardia, or nausea; advise patients to sit or lie down for first several doses if necessary; administer where patient can sit or lie down if necessary

    May cause hypercalcemia; not recommended with preexisting hypercalcemia or in patients who have an underlying hypercalcemic disorder (eg, primary hyperparathyroidism) because of the possibility of exacerbating hypercalcemia

    May cause hypercalciuria; unknown whether the drug may exacerbate urolithiasis in patients with active or a history of urolithiasis; if active urolithiasis or preexisting hypercalciuria is suspected, consider measuring urinary calcium excretion

    Pregnancy

    Not indicated for females of reproductive potential

    Lactation

    Not indicated for females of reproductive potential

    Adults

    80 mcg/day subcutaneously.

    Geriatric

    80 mcg/day subcutaneously.

    Adolescents

    Safety and efficacy have not been established.

    Children

    Safety and efficacy have not been established.

    Infants

    Safety and efficacy have not been established.

    abaloparatide

    solution for SC injection

    • 80mcg/40mcL (prefilled pen delivers 30 daily doses of 80mcg)