نتایج جستجو برای: national drug file
تعداد نتایج: 1011377 فیلتر نتایج به سال:
Background: The aim of this study was to estimate the prevalence of clinical hyperthyroidism at the national and sub-national levels using the claims data. Methods: National anti-thyroid medications (methimazole and propylthiouracil) sales data in 2014 were extracted from pharmaceutical sales data that were reported by Iran's Food and Drug Administration (FDA). By using prescriptions data of S...
The Smoke and Mirrors File System (SMFS) mirrors files at geographically remote datacenter locations with negligible impact on file system performance at the primary site, and minimal degradation as a function of link latency. It accomplishes this goal using wide-area links that run at extremely high speeds, but have long round-trip-time latencies—a combination of properties that poses problems...
In order to ensure the safety of parenterals, international pharmacopoeias and national standards have set up stringent guidelines and standards. Particulate con- tamination is a potential health risk caused by intravenous injection of particles large enough to potentially clog the small arteries. Particles could be produced through manufacturing and packaging or even dispensing of the ph...
Improper drug prescription by physicians due to wrong diagnosis, wrong drug choise or other causes will waste national funds. The annual drug costs in Iran is 900 billions Rials. With approvement of prescription, it can be reduced to 500 billions Rials. Effective factors in costs reduction are: 1) Increasing medical knowledge and persistent education of physicians. 2) Spending more time for eac...
سابقه و هدف: ابزار چرخشی pathfile، اخیراً، برای پیش آماده سازی کانال ها به صورت مکانیکی ارائه شده و گفته می شود مزایای متعددی در این درمان ها به همراه دارد. تحقیق حاضر با هدف تعیین موارد شکست فایل در پیش آماده سازی کانال با استفاده از فایل دستی و pathfile در سیستم روتاری protaper انجام شد. مواد و روشها: در یک تحقیق تجربی آزمایشگاهی، 100 بلوک آکریلی با انحنای یکسان و طول کارکرد برابر انتخاب و به ...
When an innovative (brand-name) drug is going off patent protection, the innovative drug companies and/or generic drug companies may file an abbreviated new drug application (ANDA) for generic approval through the conduct of a bioequivalence study. Bioequivalence testing for generic approval is based on the Fundamental Bioequivalence Assumption that when two drug products have similar drug abso...
Out-of-date or incomplete drug product labeling information may increase the risk of otherwise preventable adverse drug events. In recognition of these concerns, the United States Federal Drug Administration (FDA) requires drug product labels to include specific information. Unfortunately, several studies have found that drug product labeling fails to keep current with the scientific literature...
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