Rimantadine

From Proteopedia

Revision as of 12:30, 6 December 2010 by David Canner (Talk | contribs)
Jump to: navigation, search

Rimantadine, also known as Flumadine

Drag the structure with the mouse to rotate

Better Known as: Flumadine

  • Marketed By: Forest Labs
  • Major Indication: Influenza Infection
  • Drug Class: M2 Proton Channel Inhibitor
  • Date of FDA Approval (Patent Expiration): 1993 (2001)
  • 1994 Sales: N/A
  • Importance: One of the the first treatments for Influenza Infections. Since 1994, nearly 100% of influenza viruses had developed resistance to rimantadine, and it is no longer recommended as a treatment for the flu.
  • The following is a list of Pharmacokinetic Parameters. See: Pharmaceutical Drugs for more information

Mechanism of Action

Pharmacokinetics

M2 Proton Channel Inhibitor Pharmacokinetics[1]
Parameter Rimantadine Amantadine
Tmax (hr) 4.3 Amantadine
Cmax (ng/ml) 310 Amantadine
Bioavailability (%) >90 >90
Protein Binding (%) 40 67
T1/2 (hr) 27.7 ~15
AUC (ng/ml/hr) 11917 Amantadine
Clearance (L/h) Rimantadine Amantadine
Dosage (mg) 100 Amantadine
Metabolism Rimantadine Amantadine

References

  1. Anderson EL, Van Voris LP, Bartram J, Hoffman HE, Belshe RB. Pharmacokinetics of a single dose of rimantadine in young adults and children. Antimicrob Agents Chemother. 1987 Jul;31(7):1140-2. PMID:3662473


Proteopedia Page Contributors and Editors (what is this?)

David Canner, Alexander Berchansky

Personal tools