Food and Drug Administration Action Against Homeopathic Teething Tablets Lacked Evidence Base
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چکیده
منابع مشابه
United States Food and Drug Administration Drug Approval summary: Gefitinib (ZD1839; Iressa) tablets.
On May 5, 2003, gefitinib (Iressa; ZD1839) 250-mg tablets (AstraZeneca Inc.) received accelerated approval by the United States Food and Drug Administration as monotherapy for patients with locally advanced or metastatic non-small cell lung cancer after failure of both platinum-based and docetaxel chemotherapies. Information provided in this summary includes chemistry manufacturing and controls...
متن کاملReport from the FDA United States Food and Drug Administration Drug Approval Summary: Gefitinib (ZD1839; Iressa) Tablets
On May 5, 2003, gefitinib (Iressa; ZD1839) 250-mg tablets (AstraZeneca Inc.) received accelerated approval by the United States Food and Drug Administration as monotherapy for patients with locally advanced or metastatic non-small cell lung cancer after failure of both platinumbased and docetaxel chemotherapies. Information provided in this summary includes chemistry manufacturing and controls,...
متن کاملClinical evidence supporting pharmacogenomic biomarker testing provided in US Food and Drug Administration drug labels.
IMPORTANCE Genetic biomarkers that predict a drug's efficacy or likelihood of toxicity are assuming increasingly important roles in the personalization of pharmacotherapy, but concern exists that evidence that links use of some biomarkers to clinical benefit is insufficient. Nevertheless, information about the use of biomarkers appears in the labels of many prescription drugs, which may add con...
متن کاملQualitative Evaluation of Laboratory hoods in Campus Laboratory and Food and Drug Administration of Qazvin University of Medical Sciences and taking intervential action
Background and Objective: various type of chemical and biological agent with different health effect are used in laboratorial environment. Some researches indicated the risk of respiratory exposure in university laboratories. Present study aims to evaluate the operation of laboratorial hoods in campus and food and drug organization in Qazvin University of medical science. Materials and Metho...
متن کاملNew food safety initiatives in the Food and Drug Administration.
Concern over the presence of veterinary drug residues in food has been increasing world wide. Because of this concern the Food and Drug Administration's Center for Veterinary Medicine (CVM) has been involved on an international basis in efforts to develop food safety standards for veterinary drugs. The major thrust of the Codex Committee on Residues of Veterinary Drugs in Foods (CC/RVDF) has be...
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ژورنال
عنوان ژورنال: Alternative and Complementary Therapies
سال: 2018
ISSN: 1076-2809,1557-9085
DOI: 10.1089/act.2017.29148.ble