| Drug Name (select from list of drugs shown) |
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| Patient Information |
| Patient Name: |
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| Patient ID: |
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| Patient Group No.: |
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| Patient DOB: |
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| Prescribing Physician |
| Physician Name: |
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| Physician Phone: |
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| Physician Fax: |
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| Physician Address: |
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| City, State, Zip: |
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| Please circle the appropriate answer for each question. |
| 1. |
Is the physician purchasing and providing the drug “incident to” physician services (i.e., drugs supplied and administered by a physician or under a physician’s direct supervision)? |
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"Medicare Close as B: Drug should be covered under Medicare Part B. Please select the appropriate Close as B outcome." |
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[If the answer to this question is yes, then no further questions required.] |
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| 2. |
Is the patient in a long-term care (LTC) bed that is covered by Medicare? |
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| 3. |
Is the request for one of the following drugs via an IV infusion pump? |
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Acyclovir / Foscarnet / Amphotericin B / Flurouracil / Cytarabine / Bleomycin / Doxorubicin / Vincristine / Vinblastine / Treprostinil (Remodulin) / Cisplatin / Gemcitabine / Oxaliplatin / Morphine |
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| 4. |
Does the patient have a diagnosis of: |
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Postmenopausal osteoporosis OR / Primary (idiopathic) or hypogonadal osteoporosis OR / Glucocorticoid-induced osteoporosis |
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[If no, no further questions.] |
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| 5. |
Does the patient have a history of osteoporotic fracture? |
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[If yes, skip to question 9.] |
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| 6. |
Does the patient have greater than 1 risk factor for fracture? |
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Advanced age (postmenopausal women and men greater than 50 years of age) / Low body mass index (less than 19 kg/m2) / Parental history of hip fracture / Current smoking / Alcohol intake of 3 or more drinks per day / Glucocorticoid therapy (greater than or equal to 5 mg/day prednisone or equivalent for greater than or equal to 3 months) / Rheumatoid arthritis / Secondary causes of osteoporosis |
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[If yes, skip to question 9.] |
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| 7. |
Has the patient had an inadequate response to a bisphosphonate trial of a minimum of one year? |
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[If yes, skip to question 9.] |
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| 8. |
Is a trial of a bisphosphonate contraindicated or was the patient intolerant to a trial of bisphosphonate therapy? |
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[If no, no further questions.] |
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| 9. |
Does the patient have ANY of the following contraindications or exclusions to Forteo therapy? |
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Paget’s disease of bone / Unexplained elevations of alkaline phosphatase / Open epiphyses (ie, pediatric or young adult patient) / Prior radiation therapy involving the skeleton / History of a skeletal malignancy / Bone metastases / Pre-existing hypercalcemia / Metabolic bone disease other than osteoporosis |
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[If yes, no further questions.] |
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| 10. |
Has the patient been on Forteo therapy for less than 24 months and will Forteo be discontinued after a total of 24 months of treatment? |
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[If no, no further questions.] |
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| 11. |
Will the patient be receiving bisphosphonate therapy concurrent with Forteo therapy? |
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I affirm that the information given on this form is true and accurate as of this date.
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