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NACCT 2016


TUE800 - ACMT Pre-Symposium: New and Novel Rx Drugs, Antidotes, and Delivery Systems


Sep 13, 2016 8:00am ‐ Sep 13, 2016 12:00pm

Description

Ed Silverman, BA, MS
Pharmalot: Insights From a Pharmaceutical Investigative Journalist
Objecitves:

  • Highlight processes used by the government to regulate drug marketing and pricing
  • Discuss notable examples within the pharmaceutical industry

Jeanmarie Perrone, MD
Confidential Briefing: An Inside Look at an FDA Advisory Committee
Objectives:

  •  Describe the opportunities for medical toxicologists to impact drug safety in the drug evaluation process at the FDA

  • Examine the pharmaceutical industry maneuvers to influence advisory committee outcomes

David Wood, MD
British FDA: Naughty or NICE?
Objectives:

  • Understand the drug approval process in the UK
  • Discuss the pros and cons of requiring a new drug to be cost-effective

Keith Burkhart, MD
FDA Panel: Issues in the Pharmaceutical Approval and Regulatory Process
Objectives:

  • Describe the FDA decision-making process
  • Identify FDA processes to evaluate drug safety

     FDA Panel Participants:

  • Ed Silverman, BA, MA
  • David Wood, MD
  • Jeanmarie Perrone, MD
  • Keith Burkhart, MD
  • Lewis Nelson, MD


Pavan Sekhar, MD
Suggamadex: New Kid on the Block
Objectives:

  • Discuss the pharmacology of Sugammadex, explain how the FDA evaluated Sugammadex, summarize the indications and contraindications of Sugammadex 
  • Compare and contrast Sugammadex with other neuromuscular blocker reversal agents

Christina Hantsch Bardsley, MD
Icati"banter" - A Formulary Debate
Objectives:

  • Identify the pros and cons of addition of Icatibant to a formulary.

Silas Smith, MD
5-FU’d: Uridine Triacetate Use in Pyrimidine Analogue Toxicity
Objectives:

  • Explain manifestations of fluorouracil or capecitabine toxicity
  • Discuss the use of uridine triacetate in fluorouracil or capecitabine overdose or toxicity

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