| 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. |
Does the patient have the diagnosis of anorexia associated with weight loss in AIDS? |
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[If the answer to this question is no, skip to question 7.] |
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| 2. |
Has the patient had an involuntary weight loss of greater than 10 percent of pre-illness baseline body weight or body mass index (BMI) less than 20 kg per square meter in the absence of a concurrent illness or medical condition other than Human Immunodeficiency Virus (HIV) infection that may cause weight loss? |
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[If the answer to this question is no, no further questions required.] |
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| 3. |
Has the patient demonstrated an inadequate treatment response to a 30-day drug regimen of megestrol acetate (Megace)? |
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[If the answer to this question is yes, skip to question 5.] |
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| 4. |
Does the patient have a contraindication to or been intolerant to megestrol acetate (Megace)? |
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[If the answer to this question is no, no further questions required.] |
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| 5. |
Has the patient previously received Marinol therapy? |
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[If the answer to this question is no, no further questions.] |
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| 6. |
Has the patient demonstrated a positive response to Marinol therapy by maintaining or increasing his initial weight and/or muscle mass? |
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[No further questions required.] |
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| 7. |
Does the patient have a diagnosis of nausea and vomiting associated with cancer chemotherapy? |
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[If the answer to this question is no, no further questions required.] |
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| 8. |
Is the patient receiving a chemotherapy or radiation regimen? |
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[If the answer to this question is no, no further questions required.] |
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| 9. |
Has the patient, through at least one cycle of chemotherapy, experienced an inadequate treatment response to or intolerance to intravenous Zofran and at least one of the following anti-emetic agents: metoclopramide, promethazine, prochlorperazine, meclizine, trimethobenzamide, or oral 5-HT3 receptor antagonists (e.g. Zofran, Kytril)? |
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[If the answer to this question is no, no further questions required.] |
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| 10. |
Has the patient received previous Marinol therapy? |
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[If the answer to this question is no, no further questions.] |
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| 11. |
Has the patient shown a positive response to Marinol therapy by showing a reduced incidence of emesis and/or nausea? |
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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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