In patients with severe renal impairment. Hypocalcemia: Hypocalcemia may worsen with the use of Prolia ®, especially Other clinically significant allergic reaction occurs, initiate appropriate therapy and Tightness, facial and upper airway edema, pruritus, and urticaria. Symptoms have included hypotension, dyspnea, throat Hypersensitivity: Clinically significant hypersensitivity including anaphylaxis hasīeen reported with Prolia ®. Patients receiving Prolia ® should not receive Same Active Ingredient: Prolia ® contains the same active ingredient Reactions have included anaphylaxis, facial swelling and urticaria. In patients with a history of systemic hypersensitivity to any component of the product. Prior to initiating treatment with Prolia ®. In women of reproductive potential, pregnancy testing should be performed Prolia ® is contraindicated in women who are pregnant and mayĬause fetal harm. Pre-existing hypocalcemia must be corrected prior to initiating LearnĬontraindications: Prolia ® is contraindicated in patients with Prolia ® is indicated as a treatment to increase bone mass in women at high riskįor fracture receiving adjuvant aromatase inhibitor therapy for breast cancer. Patients Prolia ® also reduced the incidence of vertebral fractures. Prolia ® is indicated as a treatment to increase bone mass in men at high risk forįracture receiving androgen deprivation therapy for nonmetastatic prostate cancer. High risk of fracture is defined asĪ history of osteoporotic fracture, multiple risk factors for fracture, or patients who haveįailed or are intolerant to other available osteoporosis therapy. Systemic glucocorticoids in a daily dosage equivalent to 7.5 mg or greater of prednisone andĮxpected to remain on glucocorticoids for at least 6 months. In men and women at high risk of fracture who are either initiating or continuing Prolia ® is indicated for the treatment of glucocorticoid-induced osteoporosis Or multiple risk factors for fracture or patients who have failed or are intolerant to other Osteoporosis at high risk for fracture, defined as a history of osteoporotic fracture, Prolia ® is indicated for treatment to increase bone mass in men with Postmenopausal women with osteoporosis, Prolia ® reduces the incidence of Find a center near you to learn more about how a post-hospital stay can help you get back to active.Indicated for the treatment of postmenopausal women with osteoporosis at high risk forįracture, defined as a history of osteoporotic fracture, or multiple risk factors forįracture or patients who have failed or are intolerant to other available osteoporosis therapy. Heartland-ManorCare skilled nursing centers provide a comprehensive regime of specialized rehabilitation services, each one designed to help you achieve your recovery goal. I am now stronger and more flexible and able to walk on my own safely." - Kathleen It was important to me to be able to get around independently since I was doing everything for myself before my accident. Back to Active: "When I first arrived I wasn't able to do much on my own. The team did a home assessment to ensure Kathleen was confident in her ability to get around on her own. The therapy team helped Kathleen work on strengthening, balance and range of motion so she would feel confident returning home. The nursing team helped Kathleen manager her pain and taught her about caring for her incisions. Post-acute Stay:Īt the center, the interdisciplinary team created a care plan to help Kathleen meet her goals. She was in severe pain and had surgical incisions that required care. She required physical and occupational therapy to help get her strong enough to transfer and walk on her own. Kathleen, 74, lives on her own and gardens extensively. Post-surgery, Kathleen was unable to walk or transfer and was in need of rehabilitation and nursing care before returning home. She was was severely injured with several broken bones that required surgery. After a serious accident, Kathleen was admitted to the hospital.
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