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    Thread: Relative Safety of Ephedrine

    1. #1
      YellowJacket's Avatar
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      Default Relative Safety of Ephedrine



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      An Analysis of the Relative Safety of Ephedra
      By Doug Kalman MS, Jose Antonio, Ph.D., FACSM, and Richard
      B. Kreider, PhD,

      In an early Internet release, the Annals of Internal
      Medicine posted an upcoming brief communication concerning
      the dietary supplement ephedra (1).

      This study raised media frenzy concerning the regulatory
      status of ephedra.

      The authors utilized the Toxic Exposure Surveillance System
      (TESS) report of 2001 and compared it with ephedra sales
      data provided to them by SPINS, a market analysis firm.

      In addition, the authors also utilized a magazine report to
      approximate the total sales of ephedra within the United
      States for the year 2000 (2).

      There are several methodological and fundamental flaws with
      the design and conclusions made by Bent et al.

      The TESS raw data indicates that 55.5% of all Poison Control
      Center reports related to Ma Huang (ephedra) alone or in
      combination with another herb (multi-botanical) were in
      people under the age of 19.

      Additionally, 27.9% of all of the exposures were in children
      less than 6 years of age (3).

      This information is vital as in 7,927 exposures; the Poison
      Control Centers deemed 14% (1,178) to be an adverse
      reaction.

      In clinical research the guidelines set forth by the
      International Committee on Harmonization (ICH) defines an
      adverse reaction/event (AE) 'any untoward medical occurrence
      in a patient or clinical investigation subject administered
      a pharmaceutical product and which does not necessarily have
      to have a causal relationship with this treatment' (4).

      The TESS system defines an adverse reaction (AR) as 'an
      adverse event occurring with normal, prescribed, labeled or
      recommended use of the product, as opposed to overdose,
      misuse or abuse'.

      The TESS system also captures AR's that are 'unwanted
      effects due to an allergic, hypersensitive, or idiosyncratic
      response to the active or inactive ingredients, or
      excipients'.

      Thus, the definitions and establishment of clear causality
      or relationship is not clear within the TESS system and when
      contrasted with normal research guidelines for defining and
      AE/AR appear to be questionable.

      The Center for Drug Evaluation and Research (CDER) policy on
      AR/AE's is that accumulated case reports (AER's) cannot be
      used to calculate incidence or estimates of drug risk (5).

      This misguided calculation is exactly what the authors
      attempted to do.

      The 2001 TESS report details that the vast amount of
      exposures were unintentional (85.2%).

      In the ephedra analysis, 46.7% of the exposures were of the
      unintentional variety (using TESS definitions and data from
      table 22B).

      It cannot be downplayed that the TESS report only captured
      data on 12 known herbs, Drs. Bent et al mistakenly state
      that ephedra accounts for 64% of all herbal related adverse
      reactions, however, there are hundred of herbals sold on the
      U.S. market, not 12, thus their conclusion is overstated.

      The sales data that Drs. Bent et al utilized in an attempt
      to correlate the TESS data with sales is incomplete. The
      SPINS database does not capture data by zip code nor does it
      capture the true mass market (i.e., Walmart, Costco, GNC
      Corporate stores), thus any data generated by the SPINS
      agency is only a small snapshot of what is truly happening
      in the sales of ephedra or ephedra-related products.

      The Nutrition Business Journal estimates that in 2000,
      ephedra and ephedra related products generated
      $1,050,000,000 (6).

      Utilizing the NBJ market analysis, the best estimate is that
      26,250,000 servings (or individual capsules/tablets) of
      ephedra or ephedra related products were sold in 2000.

      The sales figures are based upon retail mass market, mail
      order, practitioners, Internet sales and natural food/health
      chain channels (6).

      In the Bent report, it is stated that an assumption was
      made that ephedra related sales were one-half of all non-
      retail herb sales and this accounted for 0.82% of herbal
      product sales.

      The confliction in detail does not make sense. It appears
      that the SPINS data is inaccurate when comparing it to the
      more comprehensive NBJ data.

      Thus, this section of the Bent paper appears to be out of
      context and unreliable.

      While we as scientists and health care providers need to
      know the evidence (direct, not computed) concerning the
      safety of ephedra or ephedra related products, we must not
      fail to use the published peer-reviewed clinical studies as
      the basis for an understanding.

      While the clinical trials are limited in subject size as
      compared to Phase III drug studies, they do give us a basis
      for understanding the potential for serious adverse events
      and what population is best suited for potential use of
      these products.

      It is clear that people under the age of 19 should not take
      this herb; there simply have been no studies in that age
      group (on the herbal ephedrine).

      The TESS data states 55.5% of all exposures were from people
      19 or younger.

      The comparison of ephedra versus other herbs inherently
      inaccurate as the TESS data only captured 12 total named
      herbs.

      Given the TESS data for ephedra reporting an adverse
      reaction rate of 14% (TESS conclusion) and a mortality rate
      of 0.000757% (comparison of 6 deaths versus 7,927
      exposures), one would expect a better comparison to be made
      using this data.

      For example with relation to kava, there was one death in
      336 exposures (0.002976%), thus we can also conclude that
      kava is 3.9 times as likely to cause death as ephedra.

      It should also be noted that the adverse reaction frequency
      was similar for Gingko biloba (13.7% vs 14%) as ephedra
      and the AR for kava was much higher (17.5%).

      Perhaps, a less negative conclusion would not serve the
      purpose of the study.

      The manipulative presentation of the data shared by Bent et
      al viewed alongside the fact that the authors have and still
      testify for plaintiff law firms on behalf of anti-ephedra
      litigation, leads to speculation that this study's intent
      was to establish their published paper as evidence that
      ephedra is dangerous.

      An informed professional audience must wonder where the
      truth actually lays. Whose future and benefit does this
      paper serve?

      Douglas S. Kalman MS, RD, FACN
      Miami Research Associates
      6280 Sunset Drive
      Suite 600
      Miami, FL. 33143

      Disclosure: Mr. Kalman has testified in cases related to
      ephedra on behalf of Cytodyne Technologies, Inc.

      Jose Antonio, Ph.D., FACSM
      Adjunct Professor
      Exercise Science & Health Promotion
      Florida Atlantic University
      777 Glades Road
      P. O. Box 3091
      Boca Raton, FL 33431-0991

      Richard B. Kreider, PhD, EPC, FACSM, FASEP
      Professor & Chair
      Exercise & Sport Nutrition Laboratory
      Center for Exercise, Nutrition, and Preventive Health
      Department of Health, Human Performance & Recreation
      Baylor University
      PO Box 97313
      Waco, TX 76798-7313

      Disclosure: Dr. Kreider has served as an expert in
      litigation for Metabolife.

      References:

      1) Bent S, Tiedt TN, Odden MC, Shiplak MG. The relative
      safety of ephedra compared with other herbal products. Ann
      Intern Med 2003;138:000-000.
      www.acponline.org/journals/annals/ephedra.htm
      Accessed online February 5, 2003

      2) Richman A, Witkowski JP. 7th Annual Herb Sales Survey.
      Whole Foods Magazine. 2001:23-30.

      3) Litovitz TL, Klein-Schwartz W, Rodgers GC, Cobaugh DJ,
      Youniss J, Omslauer JC, May ME, Woolf AD, Benson BE. 2001
      Annual report of the American Association of Poison Control
      Centers Toxic Exposure Surveillance System. Amer J Emerg Med
      2002;20(5):391-452.

      4) Cohen A, Posner J. A Guide to Clinical Drug Research. 2nd
      edition Kluwer Academic Publishers 2002. Pp XI, 34,-35, 154.

      5) www.fda.gov/cder/aers/ and
      https://www.fda.gov/medwatch/articles...ostrep.htm#aer
      Accessed February 18, 2003.

      6) NBJ's Supplement Business Report 2002. Penton Media, Inc.
      Pp 5-171-2,
      Figure 5-5, Figure 5-7. Available: www.nutritionbusiness.com

    2. #2
      pudgy's Avatar
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      another good one, glad to see your gonna be spending more time here

    3. #3
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      As always ... GOOD post, YJ.

    4. #4
      YellowJacket's Avatar
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      Thanks Doc. Welcome brother, great to have ya over....

    5. #5
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      Originally posted by YellowJacket
      Thanks Doc. Welcome brother, great to have ya over....
      And no credit given to me for posting this over at AM first bro?? j/k...

    6. #6
      YellowJacket's Avatar
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      Originally posted by Sheesh
      And no credit given to me for posting this over at AM first bro?? j/k...
      Hey, its not like I didnt already have it & not like every major news website didnt have it


      Thanks to Sheesh for posting this at my board


      (there)

    7. #7
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      Originally posted by YellowJacket
      Hey, its not like I didnt already have it & not like every major news website didnt have it


      Thanks to Sheesh for posting this at my board


      (there)
      LOL


    8. #8
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      good post
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