Includes investigational and herbal products in addition to prescription and over-the counter (OTC) drugs, as well as neonatal and pediatric-specific monographs. Tools include: drug identification, interactions, IV compatibility, patient ed, and comparisons. USF HEALTH ONLY Online Resource.
Database includes investigational and orphan drugs in addition to prescription & OTC. Tools include comparisons of 3000+ charts and tables, advanced dosing tools, drip rates, dont crush/chew, & look/sound alikes. USF HEALTH ONLY Online Resource.
Contains information about FDA-approved indications, off-label uses, pharmacokinetic data, safety information, pharmacology, and monitoring. Includes AHFS Drug Information. USF HEALTH ONLY Online Resource
Databases of summaries and detailed monographs for drugs and drug interactions. Also includes tools on Drug Interactions, Drug Identification, IV Compatability, Drug Comparisons, and RED BOOK online. USF HEALTH ONLY Online Resource.
Lists complementary and alternative medications along with safety, effectiveness, and interaction ratings for each based on the best scientific evidence. USF HEALTH ONLY Online Resource.
DailyMed is the official provider of FDA label information (package inserts). This Web site provides a standard, comprehensive, up-to-date, look-up and download resource of medication content and labeling found in medication package inserts.
The NLM Drug Information Portal is a free resource that searches U.S. government agencies, including the National Library of Medicine, FDA and CDC. Includes current information regarding consumer health, clinical trials, AIDS–related drug information, MeSH® pharmacological actions, PubMed® biomedical literature, and physical properties and structure. The portal covers drugs from the time they are entered into clinical trials through entry into the U.S. marketplace.
The Approved Drug Products with Therapeutic Equivalence Evaluations (also known as The Orange Book) identifies drug products approved on the basis of safety and effectiveness by the Food and Drug Administration (FDA) under the Federal Food, Drug, and Cosmetic Act.
