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Apidra

Active Ingredient(s): Insulin Glulisine Recombinant
First Approved by the FDA: April 16, 2004
Pharmaceutical Company: SANOFI AVENTIS US

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Apidra Article Summary

Insulin Glulisine Is A Rapid-acting Insulin Analogue That Differs From Human Insulin In That The Amino Acid Asparagine At Position B3 Is Replaced By Lysine And The Lysine In Position B29 Is Replaced By Glutamic Acid. Chemically, It Is 3b-lysine-29b-glutamic Acid-human Insulin, Has The Empirical Formula C258h384n64o78s6 And A Molecular Weight Of 5823. It Was Developed By Sanofi-aventis And Sold Under The Trade Name Apidra. When Injected Subcutaneously, It Appears In The Blood Earlier And At Highe ...

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This article is from Wikipedia. All text is available under the terms of the GFDL
(GNU Free Documentation License) | http://en.wikipedia.org/wiki/Apidra





Possible Dosages for this and Related Drugs:

Note: May Include Dosages for Drugs similar to Apidra

Injection   0,  100 units/ml,  1000 units/10ml (100 units/ml),  300 units/3ml (100 units/ml)
Powder   1mg/inh,  3mg/inh

Related Drug Listing(s):

  • Exubera Insulin Recombinant Human
  • Insulin Detemir
  • Levemir Insulin Detemir


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    Drugs/Apidra.asp Last Modified November 6 2008


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