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An official publication of the ACR and the ARP serving rheumatologists and rheumatology professionals

Drug Updates

  |  Issue: May 2009  |  

Michele Kaufman is a freelance medical writer based in New York City.

References

  1. Coffey J. FDA petition letter to remove propoxyphene from the market. Published December 5, 2008; www.ashp.org/DocLibrary/Advocacy/Propoxyphene.aspx. Accessed April 8, 2009.
  2. Traynor K. Close vote by FDA advisers favor propoxyphene withdrawal. Published March 2, 2009; www.ashp.org/import/news/HealthSystemPharmacyNews/newsarticle.aspx?id=3037. Accessed April 8, 2009.
  3. FDA. Transdermal drug patches with metallic backings. Published March 5, 2009; www.fda.gov/medwatch/safety/2009/safety09.htm#Transdermal. Accessed April 8, 2009.
  4. FDA. FDA warns about wearing medicated patches during MRIs. Published March 5, 2009; www.fda.gov/bbs/topics/NEWS/2009/NEW01967.html. Accessed April 8, 2009.
  5. FDA. Raptiva (efalizumab). Published April 8, 2009; www.fda.gov/medwatch/safety/2009/safety09.htm#Raptiva. Accessed April 13, 2009.
  6. Sedghizadeh PP, Stanely K, Caliguir M, Hofkes S, Lowry B, Shuler CF. Oral bisphosphonate use and the prevalence of osteonecrosis of the jaw: An institutional inquiry. J Am Dent Assoc. 2009;140:61-66.
  7. Edwards BJ, Hellstein JW, Jacobsen PL, et al. Updated recommendations for managing the care of patients receiving oral bisphosphonate therapy: An advisory statement from the American Dental Association Council on Scientific Affairs. J Am Dent Assoc. 2008;139:1674-1677.
  8. Wysowski D. Reports of esophageal cancer with oral bisphosphonate use. N Engl J Med. 2009;360:89-90.
  9. Chustecka Z. Esophageal cancer in patients taking oral bisposphonates. Published December 31, 2008; www.med scape.com/viewarticle/586127. Accessed April 8, 2009.
  10. FDA. Potential signals of serious risks/new safety information identified from the Adverse Event Reporting System (AERS) between January–March 2008. Updated February 4, 2009; www.fda.gov/Cder/aers/potential_signals/potential_signals_2008Q1.htm. Accessed April 8, 2009.
  11. Fischer A. FDA posts drugs under review over possible safety concerns. Published February 5, 2009; www.firstwordplus.com/Fws.do?articleid=AE4EA7AB7202473B8DC3548A74AA4F57&logRowId=282534. Accessed April 8, 2009.
  12. Paddock C. FDA approves first gout drug for 40 years. Published February 16, 2009. www.medicalnewstoday.com/articles/139130.php. Accessed April 8, 2009.
  13. FDA approves Genzyme’s Synvisc-One for osteoarthritis of the knee. Published February 26, 2009; www.genzyme.com/corp/investors/GENZ%20PR-022609.asp. Accessed April 8, 2009.
  14. Additional strengths of Avinza available. Published February 5, 2009. www.empr.com/Additional-strengths-of-Avinza-available/article/126905. Accessed April 8, 2009.
  15. Scytera Foam available for chronic psoriasis. Published January 26, 2009. www.empr.com/Scytera-Foam-available-for-chronic-psoriasis/article/126384. Accessed April 8, 2009.
  16. UCB receives complete response letter from US FDA for use of Cimzia in rheumatoid arthritis patients. Published January 5, 2009; www.pharmasentry.com/news/newsletter.cfm?linkid=B1776F25-1372-54C2-6119BA974B2E09CC. Accessed April 8, 2009.
  17. UCB’s meeting with U.S. FDA defines path forward for Cimzia in rheumatoid arthritis. Published February 6, 2009; www.ucb.com/news/newsdetail.asp?newsid=1287988. Accessed April 8, 2009.
  18. Acurox tablets new drug application accepted for filing with a priority review classification. Published March 3, 2009; www.globenewswire.com/newsroom/news.html?d=160640. Accessed April 8, 2009.

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