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April 2008: FDA Web Site Adds Two New Pages For Learning About Drug Safety

Some Important Terms Are Defined And Various Research Resources From FDA Are Listed

(Posted by Tom Lamb at DrugInjuryWatch.com)

On April 11, 2008 the FDA added to its web site one page that gives short definitions for some important terms used in the realm of prescription drug safety, and another page that is intended to assist one when researching medication safety issues. 

We look, first, at "A Guide to Drug Safety Terms at FDA", which begins with this introduction:

The Food and Drug Administration (FDA) approves a drug for marketing after determining that the drug's benefits of use outweigh the risks for the condition that the drug will treat. But even with a rigorous evaluation process, some safety problems surface only after a drug has been on the market and has been used in a broader population. This guide offers descriptions of some of the drug safety terms commonly used by FDA throughout the life cycle of a drug.

The drug safety terms defined on this FDA web page are organized by the different stages of a drug's history.  Here is a summary of the stages and terms found on this page:

1.  FDA REVIEW

  • Pre-Clinical Data
  • New Drug Approval Process
  • Adverse Drug Reaction

2.  TAKING MEDICATION

  • Medication Guides
  • Consumer Medication Information (CMI)
  • Prescription Drug Labeling
  • Nonprescription Drug Label ("Drug Facts")
  • Boxed Warning

3.  MONITORING AFTER APPROVAL

  • Post-Market Surveillance
  • Adverse Event Reporting System (AERS)
  • MedWatch

4.  REMOVAL FROM THE MARKET

  • Drug Recall
  • Drug Withdrawal

5.  TYPES OF SAFETY ANNOUNCEMENTS

  • Early Communication About an Ongoing Safety Review
  • Public Health Advisories
  • Letters to Health Care Professionals ("Dear Doctor" letters)
  • Information for Health Care Professionals

The second new page at the FDA site has to do with researching the safety of prescription medications; it is titled "Find the Latest Drug Product and Safety Information".

Here are some of the FDA resources for drug safety research provided on this page:

Index to Drug-Specific Information
www.fda.gov/cder/drug/drugsafety/DrugIndex.htm

Public Health Advisories
www.fda.gov/cder/news/pubpress.htm

MedWatch Alerts
www.fda.gov/medwatch/

DailyMed
http://dailymed.nlm.nih.gov

Drugs @ FDA
www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm

FDA Drug Safety Podcasts
www.fda.gov/cder/drug/podcast/default.htm

FDA Drug Safety Newsletter
www.fda.gov/cder/dsn/default.htm

FDA Consumer Health Information
www.fda.gov/consumer/default.htm

Recalls, Market Withdrawals and Safety Alerts
www.fda.gov/opacom/7alerts.html

We thank the FDA for posting these two new drug safety-related web pages -- both of which can be downloaded in an attractive brochure-like PDF for distribution.  Furthermore, we encourage you to share these FDA materials with family and friends who may have an interest in learning more about the safety of medications that they have been prescribed or are currently using.

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    • ConsumerMedSafety.org
      A portal of information provided by the Institute for Safe Medication Practices.
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      Submit a confidential report to national voluntary program.
    • NIH MedlinePlus
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    • Patient Medical Records Copying Cost Statutes
      State statutes that control what amount can be charged when patient requests their own medical records in U.S.
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