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13 mar 2019 · We used authorized generic (AG) products, which are identical in composition and appearance to brand-name products but are marketed as generics, as a control group to address this bias in an evaluation aiming to compare the effectiveness of generic versus brand medications.
Dapagliflozin, sold under the brand names Farxiga (US) and Forxiga (EU) among others, is a medication used to treat type 2 diabetes. [6] [7] [10] It is also used to treat adults with heart failure and chronic kidney disease.
Evaluation and approval procedures. The U.S. Food and Drug Administration (FDA) evaluates every generic version of a drug. The FDA approves a generic drug if studies indicate that the original brand-name drug and the generic version are essentially bioequivalent.
Pharmacology books often use drug prototypes to simplify explanations of drug classes and assist students in their learning. Table 1.3 provides an example of a drug prototype table used throughout this text.
12 gru 2022 · Use of a scoring tool to prioritize pharmaceutical class reviews allows for health systems with large formularies to systematically review all medication entities, while focusing the majority of their efforts on high-impact class reviews.
29 lip 2015 · The term ‘generic drug’ or ‘generic medicine’ is commonly understood, as defined by the World Health Organization (WHO), to mean a pharmaceutical product that is usually intended to be interchangeable with an innovator product, is manufactured without a licence from the innovator company and is marketed after the expiry date of the patent or oth...
25 kwi 2008 · This paper discusses the importance of an evidence-based formulary process and outlines the steps required for creating high-quality, evidence-based drug monographs and drug class reviews. Clinical judgments should be made, by validated evidence whenever possible.
