Romana Primus, MD | |
1 Shaws Cv, New London, CT 06320-4902 | |
(860) 447-8304 | |
(860) 443-8720 |
Full Name | Romana Primus |
---|---|
Gender | Female |
Speciality | Allergy & Immunology - Allergy |
Location | 1 Shaws Cv, New London, Connecticut |
Accepts Medicare Assignments | Does not participate in Medicare Program. She may not accept medicare assignment. |
Identifier | Type | State | Issuer |
---|---|---|---|
1558367698 | NPI | - | NPPES |
Taxonomy | Type | License (State) | Status |
---|---|---|---|
207KA0200X | Allergy & Immunology - Allergy | 030452 (Connecticut) | Primary |
208000000X | Pediatrics | 030452 (Connecticut) | Secondary |
Mailing Address | Practice Location Address |
---|---|
Romana Primus, MD 58 Twin Lakes Dr, Waterford, CT 06385-4112 Ph: () - | Romana Primus, MD 1 Shaws Cv, New London, CT 06320-4902 Ph: (860) 447-8304 |
News Archive
Emergent BioSolutions Inc. is hosting "Bioterrorism Prevention, Preparedness and Response," a forum organized for members of the North Atlantic Treaty Organization Parliamentary Assembly to raise global awareness of the importance of biopreparedness.
The European Food Safety Authority decision upholds years of research on sucralose - the sweetening ingredient in the original SPLENDA Sweeteners - that shows it to be safe and does not cause cancer.
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Patients who receive the anti-platelet medication clopidogrel following an acute coronary syndrome (such as heart attack) appear to be at greater risk of a heart attack or death in the first 90 days after stopping clopidogrel treatment, according to a study in the February 6 issue of JAMA: The Journal of the American Medical Association.
Medivation, Inc. and Astellas Pharma Inc. today announced that patient enrollment was completed on November 15, 2010 in the Phase 3 AFFIRM study of the investigational drug MDV3100, a novel, triple-acting oral androgen receptor antagonist, in patients with advanced prostate cancer who have previously been treated with chemotherapy. The companies also announced that clinical development of MDV3100 in Japan has commenced, with the initiation of patient dosing in a Phase 1-2 clinical study.
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