FDA: Lower Levels of NDMA in Ranitidine than Previously Reported
November 4th 2019Although the levels of NDMA that was found through FDA testing are much lower than the levels that a few third-party investigators claimed, the report indicated that these levels exceed what the FDA considers acceptable for these medicines.
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Cellular Respiration Significantly Increases in Patients with Primary Immunodeficiency Disorders
October 28th 2019Metabolic activity in the immune cells of patients with primary immunodeficiency was used as a biomarker due to cellular metabolism, which serves as a key regulator in immune cells.
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FDA Biosimilar Action Plan Presented at NASP 2019 Annual Meeting
October 22nd 2019During the 2019 National Association of Specialty Pharmacy Annual Meeting and Expo, Ron Lanton III, Esq, reviewed the FDA Biosimilars Action Plan, its implications for the biosimilar marketplace, recent legislation set to influence the biosimilar pathway and drug accessibility, and the future of the biosimilar market.
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NASP Session Explores FDA-Approved Treatment Options for AML, MM
October 19th 2019In "2019 State of Care: Oncology/ Hematology,” during the National Association of Specialty Pharmacy 2019 Annual Meeting and Expo in Washington, DC, Joseph Barone, PharmD, BCOP, examined current standards of care for acute myeloid leukemia (AML) and multiple myeloma (MM) and identified new agents approved over the past year.
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