Showing 61 - 80 results of 301 for search '"Food and Drug Administration"', query time: 0.05s Refine Results
  1. 61

    Healthy Eating: Understanding the Nutrition Facts Label by Linda Bobroff, Karla P. Shelnutt

    Published 2017-08-01
    “… The U.S. Food and Drug Administration (FDA) requires that most food packages have the Nutrition Facts label. …”
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    Article
  2. 62

    How the Veterinary Feed Directive Affects Cattle Owners by Matt Hersom, Todd Thrift, Joel Yelich

    Published 2016-08-01
    “… The Veterinary Feed Directive (VRD) is a federal regulation from the Food and Drug Administration that will change the additives that can be included in animal feed, the ways in which cattle producers manage their animals and veterinarians interact with cattle owners, and the products available for use on the ranch. …”
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    Article
  3. 63

    How the Veterinary Feed Directive Affects Cattle Owners by Matt Hersom, Todd Thrift, Joel Yelich

    Published 2016-08-01
    “… The Veterinary Feed Directive (VRD) is a federal regulation from the Food and Drug Administration that will change the additives that can be included in animal feed, the ways in which cattle producers manage their animals and veterinarians interact with cattle owners, and the products available for use on the ranch. …”
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    Article
  4. 64

    Rivaroxaban: Expanded Role in Cardiovascular Disease Management—A Literature Review by Muhammad Ajmal, Jacob Friedman, Qurat Ul Ain Riaz Sipra, Tom Lassar

    Published 2021-01-01
    “…Direct oral anticoagulants (DOACs) are widely used for the prevention of stroke in nonvalvular atrial fibrillation, treatment of deep venous thrombosis and pulmonary embolism, and as prophylaxis after hip and knee surgery after approval by the Food and Drug Administration. In the last decade, DOACs were studied for various indications; this review is focused on rivaroxaban, a factor Xa inhibitor, which is used in an expanded evidence-based fashion for coronary artery disease, peripheral artery disease, heart failure, malignancy, and prophylaxis of deep venous thrombosis in acute medical illnesses.…”
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  5. 65

    Anti-Nutritional Factors and Potassium Bromate Content in Bread and Flour Samples in Uyo Metropolis, Nigeria by A. S. Ekop, I. B. Obot, E. N. Ikpatt

    Published 2008-01-01
    “…The potassium bromate content was minimal in all the bread and flour samples and within safe limits of residual bromide found in flour as specified by the US Food and Drug Administration. The concentrations of the anti-nutritional factors in the bread and flour samples were partially different from each other when subjected to the students t-test statistics.…”
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  6. 66

    Vancomycin-Associated Leukocytoclastic Vasculitis by Makhawadee Pongruangporn, David J. Ritchie, Dongsi Lu, Jonas Marschall

    Published 2011-01-01
    “…Vancomycin is U.S. Food and Drug Administration (FDA) approved for treatment of serious infections caused by methicillin-resistant Staphylococcus aureus (MRSA) or in individuals who have failed, cannot tolerate, or are allergic to other antibiotics. …”
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  7. 67

    Capture réglementaire en temps de pandémie by Samira Guennif

    Published 2021-02-01
    “…In the midst of the covid-19 pandemic, the Food and Drug Administration (FDA) published in March the orphan drug status granted to remdesivir, a molecule patented by Gilead as a treatment for the new coronavirus. …”
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  8. 68
  9. 69

    The interaction between nirmatrelvir/ritonavir and sirolimus: a case report of a kidney recipient with renal insufficiency and COVID-19 by Yinhua Gong, Dan Shen, Jinfang Shi, Ye Jiang, Jie Gao

    Published 2025-01-01
    “…Nirmatrelvir/ritonavir is a novel drug combination authorized by the US Food and Drug Administration for the treatment of coronavirus disease 2019 (COVID-19). …”
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    Article
  10. 70

    Nonsteroidal Anti-Inflammatory Drugs for Retinal Disease by Scott D. Schoenberger, Stephen J. Kim

    Published 2013-01-01
    “…In recent years, the US Food and Drug Administration has approved new topical NSAIDs and previously approved NSAIDs have been reformulated. …”
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  11. 71
  12. 72

    Evaluating the Safety and Usability of an Over-the-Counter Medical Device for Adults With Mild to Moderate Hearing Loss: Formative and Summative Usability Testing by Megan Elizabeth Salwei, Shilo Anders, Carrie Reale, Jason M Slagle, Todd Ricketts, Matthew B Weinger

    Published 2025-01-01
    “…ObjectiveWe evaluated the safety and usability of an over-the-counter hearing aid prior to Food and Drug Administration approval and market release. …”
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  13. 73
  14. 74

    Maximizing the Survival of Amyotrophic Lateral Sclerosis Patients: Current Perspectives by Osama A. Khairoalsindi, Ahmad R. Abuzinadah

    Published 2018-01-01
    “…The disease has a poor prognosis, with only two disease-modifying drugs approved by the United States Food and Drug Administration (FDA). The approved drugs for the disease have very limited survival benefits. …”
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  15. 75

    IS IT POSSIBLE TO USE BEVACIZUMAB BIOSIMILAR IN ALL INDICATIONS REGISTERED FOR ORIGINAL DRUG? by S. V. Orlov, N. L. Shimanovskii, S. N. Fogt

    Published 2016-06-01
    “…Currently, the European Medicines Agency (EMA) and the Food and Drug Administration (FDA) have identified specific conditions under which for biosimilars extrapolation of indications is possible. …”
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  16. 76

    Sugammadex-Associated Hypotension, Bradycardia, Asystole, and Death by Kazim Mirza, Kathryn Landoski, Dilip Thakar, Jagtar Heir-Singh, Timothy Jackson, Cynthia Kassab

    Published 2020-01-01
    “…On December 16, 2015, the Food and Drug Administration (FDA) in the United States approved sugammadex (Bridion, Merck and Co), a modified gamma-cyclodextrin, to be used as a reversal agent. …”
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  17. 77

    Progress in Managing Heart Failure: an in-depth Review of Sacubitril/Valsartan Combination Therapy by Neeraj Hiremath, Jayasheela S. Hiremath, Sanatkumar B. Nyamagoud, Agadi Hiremath Viswanatha Swamy

    Published 2024-04-01
    “…The United States Food and Drug Administration has approved the drug’s use in treating patients with chronic heart failure with reduced ejection fraction (HFrEF). …”
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  18. 78
  19. 79

    Pharma TARP: A Troubled Asset Relief Program for Novel, Abandoned Projects in the Pharmaceutical Industry by Tamas Bartfai, Graham Vaughan Lees

    Published 2011-01-01
    “…The authors propose a radical response by the U.S. government and the National Institutes of Health to rescue these abandoned projects, and to continue selected programs for drug approval by the U.S. Food and Drug Administration and the European Medicines Agency. …”
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