Drugs

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Drug Information

  • American Society of Health-System Pharmacists (ASHP).
  • British National Formulary (BNF)
  • Apelon Medical Terminology
  • Drug Watch.  DrugWatch.com is a comprehensive Web site database featuring extensive information about thousands of different medications and drugs currently on the market or previously available worldwide. DrugWatch.com includes up-to-date information about prescription and over-the-counter medications and includes details about associated side effects to aid in the protection of patients and consumers.
  • DrugBank. The DrugBank database is a unique bioinformatics and cheminformatics resource that combines detailed drug (i.e. chemical, pharmacological and pharmaceutical) data with comprehensive drug target (i.e. sequence, structure, and pathway) information
  • DrugAlert.org DrugAlert.org is a comprehensive database featuring information and news alerts about potentially dangerous drugs currently on the market or previously available worldwide. The Web site is dedicated to keeping the public informed about drug recalls, side effects, and pending litigation associated with various drugs and their manufacturers

  • European Drug Utilisation Research Group (EuroDURG)

  • European Pharmaceutical Market Research Association (EphMRA)

  • FDA U.S. Food and Drug Administration.
  • FirstDataBank. First DataBank drives patient safety and healthcare quality by providing drug databases within information systems. We partner with our system developer customers to integrate our drug databases to improve user workflow, enhance clinical decision making at the point-of-need, and help reduce the incidence of medication errors and adverse drug events
  • International Society fro Pharmacoepidemiology (ISPE)
  • Medine Plus.
  • Medi-Span
  • Micromedex
  • Multum Lexicon. Product of Cerner
  • National Drug Code Directory. Drug products are identified and reported using a unique, three-segment number, called the National Drug Code (NDC), which is a universal product identifier for human drugs.  FDA inputs the full NDC number and the information submitted as part of the listing process into a database known as the Drug Registration and Listing System (DRLS), which is transforming into the electronic system (eDRLS). On a monthly basis, FDA extracts some of the information from the DRLS data base (currently, properly listed marketed prescription drug products and insulin) and publishes that information in the NDC Directory
  • NDDF Plus, A Product of FirstDataBank
  • Norwegian Institute of Public Health
  • RxNorm.RxNorm, a standardized nomenclature for clinical drugs and drug delivery devices, is produced by the National Library of Medicine (NLM). In this context, a clinical drug is a pharmaceutical product given to (or taken by) a patient with a therapeutic or diagnostic intent. A drug delivery device is a pack that contains multiple clinical drugs or clinical drugs designed to be administered in a specified sequence. In RxNorm, the name of a clinical drug combines its ingredients, strengths, and/or form.
  • WHO Collaborating Centre for International Drug Monitoring (UMC)
  • World Health  Organization (WHO)

Drug Safety

Toxicology, hazardous chemicals, environmental health, and toxic releases

 

See InHCc Section on Medication

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