Results 21 to 30 of about 229,900 (153)
Pharmaceutics, 2022 Understanding possible follow-up actions on in vitro findings helps determine the necessity of labeling for drug interactions. We analyzed information for in vitro findings on transporter-mediated interactions of drugs approved by the U.S.
Kyeong-Ryoon Lee +4 more
doaj +1 more source
A Comparative Study of Drug Package Inserts of High Selling Cardiac Drugs against the Drug Regulations of Iranian Food and Drug Administration [PDF]
Taṣvīr-i salāmat, 2019 Background and Objectives: The Drug Package Insert (PI) is a written information provided by drug manufacturers to deliver essential information for the consumer.
Sedigheh Mirzadeh Qasabeh +1 more
doaj
Current practices in organization of anesthesia drug tray
Asian Journal of Medical Sciences, 2022 Background: The risk of medication error is high in the operating room, since the anesthesiologist prepares, stores, and administers the medication. Poor labeling practices and cluttered drug trays increase the risk of syringe swap and medication error ...
Sowmya Jois +4 more
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GPCR structural characterization by NMR spectroscopy in solution
Acta Biochimica et Biophysica Sinica, 2022 In the human proteome, 826 G-protein-coupled receptors (GPCRs) interact with extracellular stimuli to initiate cascades of intracellular signaling. Determining conformational dynamics and intermolecular interactions are key to understand GPCR function as
Yang Lingyun +2 more
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Разработка и регистрация лекарственных средств, 2021 Introduction. This publication describes the design and implementation sequence of technological procedures for labeling immunobiological medicinal products produced by the FGHI RusRAPI "Microbe" of the Rospotrebnadzor.
A. V. Komissarov +9 more
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Frontiers in Pharmacology, 2022 Introduction: Regulatory agencies encourage the incorporation of the patient voices throughout clinical drug development. Patient-Reported Outcomes (PROs) offer one way of doing this and their use has markedly increased in many therapeutic areas ...
David Cella +8 more
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Packaging and Labeling of Pharmaceutical Products Obtained from the Internet
Journal of Medical Internet Research, 2011 BackgroundFor patients, the prescription container label may be the only source of instructions on how to take their medicines. In the United States, the legal requirements for a prescription label are set by federal law and state statutes. The container
Veronin, Michael
doaj +1 more source
Label-free drug discovery [PDF]
Frontiers in Pharmacology, 2014 Current drug discovery is dominated by label-dependent molecular approaches, which screen drugs in the context of a predefined and target-based hypothesis in vitro. Given that target-based discovery has not transformed the industry, phenotypic screen that identifies drugs based on a specific phenotype of cells, tissues, or animals has gained renewed ...
openaire +3 more sources
Level of Evidence Associated with FDA Safety Communications with Drug Labeling Changes: 2010-2014
INNOVATIONS in Pharmacy, 2017 Purpose: Approximately 800,000 safety reports are submitted to the FDA annually, however, only significant issues generate drug safety communications (DSC). The purpose of this study was to determine the type of clinical evidence used to warrant a change
Benjamin Hixon +4 more
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Epidemiology, Biostatistics and Public Health, 2014 Background: The use of over-the-counter (OTC) drugs has increased tremendously, however, information on risk perception regarding the use of OTC drugs and their potential toxicity is scarce.
Sunil Mathur, Neha Singh, Katie Suda
doaj +1 more source