| Elizabeth Henderika Wiggins, OTRL | |
|
6551 Park Of Commerce Blvd, Suite 200, Boca Raton, FL 33487-8218 | |
| (800) 347-2264 | |
| Not Available |
| Full Name | Elizabeth Henderika Wiggins |
|---|---|
| Gender | Female |
| Speciality | Occupational Therapist |
| Location | 6551 Park Of Commerce Blvd, Boca Raton, Florida |
| Accepts Medicare Assignments | Does not participate in Medicare Program. She may not accept medicare assignment. |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1144438474 | NPI | - | NPPES |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 225X00000X | Occupational Therapist | OT10085 (Florida) | Primary |
| Mailing Address | Practice Location Address |
|---|---|
| Elizabeth Henderika Wiggins, OTRL 1242 Golden Ln, Orlando, FL 32804-7123 Ph: (407) 928-1416 | Elizabeth Henderika Wiggins, OTRL 6551 Park Of Commerce Blvd, Suite 200, Boca Raton, FL 33487-8218 Ph: (800) 347-2264 |
News Archive
Xanodyne Pharmaceuticals, Inc., an integrated specialty pharmaceutical company with both development and commercial capabilities focused on women's healthcare and pain management, announced today that Lysteda(TM) (tranexamic acid) oral tablets has received U.S. Food and Drug Administration (FDA) approval for treatment of women suffering from cyclic heavy menstrual bleeding (HMB), also known as menorrhagia.
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Inter Press Service examines HIV in the Caribbean, where "the HIV burden varies considerably among and within countries" in the region. "'I think the prevention programs in many countries are not reaching the right people,' Michel de Groulards, regional program adviser of the UNAIDS Caribbean Regional Support Team, told IPS," the news service writes, adding, "One factor, de Groulards believed, may be that after 25 years of providing treatment, some countries have reached a plateau.
Exalenz Bioscience, a leader in developing and marketing non-invasive medical devices for diagnosing and monitoring a range of gastrointestinal and liver diseases, today announced the initiation of a clinical study designed to investigate its BreathID test to non-invasively detect primary liver cancer, also known as Hepatocellular Carcinoma (HCC).
Allergan plc today announced the U.S. Food and Drug Administration has approved the company's supplemental new drug application (sNDA) to update the label for TEFLARO (ceftaroline fosamil) for the treatment of adult patients with acute bacterial skin and skin structure infections (ABSSSI) and community-acquired bacterial pneumonia (CABP).
› Verified 7 days ago
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