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A package insert is a document included in the package of a medication that provides information about that drug and its use. For prescription medications , the insert is technical , providing information for medical professionals about how to prescribe the drug.
DailyMed is a website operated by the U.S. National Library of Medicine (NLM) to publish up-to-date and accurate drug labels (also called a "package insert") to health care providers and the general public. The contents of DailyMed is provided and updated daily by the U.S. Food and Drug Administration (FDA). The FDA in turn collects this ...
In the United States, a boxed warning (sometimes "black box warning", colloquially) is a type of warning that appears near the beginning of the package insert for certain prescription drugs, so called because the U.S. Food and Drug Administration specifies that it is formatted with a 'box' or border around the text [1] to emphasize it is of ...
Several postmarketing reports of pancreatitis (some fatal) have been made in people treated with sitagliptin and other DPP-4 inhibitors, [23] [24] and the US FDA package insert carries a warning to this effect, [2] although the causal link between sitagliptin and pancreatitis has not yet been fully substantiated. [25]
National Institutes of Technology (NIT), IIEST Shibpur are declared as Institutes of National Importance through the National Institutes of Technology, Science Education and Research Act, 2007 and its subsequent amendments.
Indian Institute of Engineering Science and Technology, Shibpur (pronunciation ⓘ) (abbr. IIEST Shibpur) is a public technological university located at Shibpur, Howrah, West Bengal, India. Founded in 1856, [ 3 ] it is recognised as an Institute of National Importance under Ministry of Education by the Government of India .
Family and friends are back at home and work following the holiday weekend, but fridges may still be packed full of Thanksgiving leftovers.For folks wondering how long the turkey, potatoes and ...
In the United States, indications for medications are regulated by the Food and Drug Administration (FDA), and are included in the package insert under the phrase "Indications and Usage". The European Medicines Agency ( EMA ) holds this responsibility for centrally authorized drugs in the European Union .