| Full Name | Bitcure |
|---|---|
| Speciality | Nurse Practitioner - Family |
| Location | 4750 Ashwood Drive, Blue Ash, Ohio |
| Authorized Official Name and Position | Ashley Dishion (NURSE PRACTITIONER) |
| Authorized Official Contact | 5133716541 |
| Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
| Mailing Address | Practice Location Address |
|---|---|
| Bitcure 4750 Ashwood Drive Blue Ash OH 45241 Ph: (855) 248-2873 | Bitcure 4750 Ashwood Drive Blue Ash OH 45241 Ph: (855) 248-2873 |
| NPI Number | 1225804560 |
|---|---|
| Provider Enumeration Date | 11/28/2023 |
| Last Update Date | 11/28/2023 |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1225804560 | NPI | - | NPPES |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 1041C0700X | Social Worker - Clinical | (* (Not Available)) | Secondary |
| 363LF0000X | Nurse Practitioner - Family | (* (Not Available)) | Primary |
News Archive
Democrats and Republicans aren't just fighting each other, they're also dealing with intra-party squabbles over the latest plan to come together to find an accord to fix the nation's budget woes. The decisions are sure to involve Medicare as a 29-member panel has until Dec. 13 to reach an agreement to present.
Amgen Inc. today announced that the U.S. Food and Drug Administration (FDA) has evaluated the content of the Company's Complete Response submission for Prolia™ (denosumab) in the treatment of postmenopausal osteoporosis and classified it as a Class 2 resubmission. With the Class 2 designation, the FDA set a corresponding Prescription Drug User Fee Act (PDUFA) action date of July 25, 2010.
A compound found in marijuana won't make you high but it may help keep your eyes healthy if you're a diabetic, researchers say.
Amylin Pharmaceuticals, Inc. and Takeda Pharmaceutical Company Limited announced today that the companies have selected the combination treatment of pramlintide, an analog of the natural hormone amylin, and metreleptin, an analog of the natural hormone leptin, for advancement toward Phase 3 development. The decision to advance the program followed encouraging results from a 52-week blinded, placebo-controlled Phase 2 extension study. The pramlintide/metreleptin combination met the key target criteria of sustained and robust weight loss.
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