| Dr Anahita Yousefi, DC | |
|
3 Washington Cir Nw Ste G, Washington, DC 20037-2326 | |
| (202) 452-1888 | |
| Not Available |
| Full Name | Dr Anahita Yousefi |
|---|---|
| Gender | Female |
| Speciality | Chiropractor |
| Location | 3 Washington Cir Nw Ste G, Washington, District Of Columbia |
| Accepts Medicare Assignments | Does not participate in Medicare Program. She may not accept medicare assignment. |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1285125302 | NPI | - | NPPES |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 111N00000X | Chiropractor | 030043 (District Of Columbia) | Primary |
| Mailing Address | Practice Location Address |
|---|---|
| Dr Anahita Yousefi, DC 3 Washington Cir Nw Ste G, Washington, DC 20037-2326 Ph: (202) 452-1888 | Dr Anahita Yousefi, DC 3 Washington Cir Nw Ste G, Washington, DC 20037-2326 Ph: (202) 452-1888 |
News Archive
Ligand Pharmaceuticals Incorporated today announced that its licensee, Onyx Pharmaceuticals, received accelerated approval from the U.S. Food and Drug Administration (FDA) for Kyprolis (carfilzomib) for Injection, a proteasome inhibitor indicated for the treatment of patients with multiple myeloma who have received at least two prior therapies, including bortezomib and an immunomodulatory agent, and have demonstrated disease progression on or within 60 days of completion of the last therapy.
As clinical studies continue to validate the use of probiotics to help promote general gastrointestinal health, a growing U.S. market for probiotics indicates that the U.S. healthcare community and consumers alike are recognizing the value of these beneficial microorganisms. However, because most probiotics are classified as dietary supplements, directing patients to the best probiotic for their individual needs can be challenging.
A Harvard study published in the New England Journal of Medicine indicates that low-income residents of three states that expanded Medicaid generally lived longer, were healthier and had better access to health care than residents of neighboring states that did not expand the program.
ViroPharma Incorporated has announced that the U.S. Food and Drug Administration (FDA) has granted fast track designation for maribavir, an oral antiviral drug candidate for the prevention of cytomegalovirus (CMV) infection in allogeneic bone marrow (stem cell) and solid organ transplant patients.
› Verified 8 days ago
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