Therapeutic Classification: bone resorption inhibitors
Pharmacologic Classification: sclerostin inhibitors
REMS
Contraindicated in:
MI or stroke in past year (↑ risk of cardiovascular death, MI, or stroke)
.Use Cautiously in:
Risk factors for cardiovascular disease
;CV: CARDIOVASCULAR DEATH, MI, peripheral edema
F and E: hypocalcemia
Local: injection site reactions
MS: arthralgia, atypical femoral fracture, muscle spasm, osteonecrosis of the jaw
Neuro: headache, insomnia, paresthesia, STROKE
Misc: HYPERSENSITIVITY REACTIONS (INCLUDING ANAPHYLAXIS AND ANGIOEDEMA)
Assess cardiac history. Avoid administration in patients who have had an MI or stroke within the preceding year. Monitor patients for signs and symptoms of emerging cardiovascular disease such as MI (chest pain, dyspnea, diaphoresis, dizziness, nausea) and stroke (unilateral weakness, slurred speech, confusion, dizziness). If MI or stroke occurs, permanently discontinue romosozumab.
Advise patients and family to call 911 and seek urgent treatment if signs and symptoms of MI or stroke (chest pain, dizziness, nausea, weakness, slurred speech, confusion, trouble breathing) occur.
NDC Code