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Larissa A. Wenning

Department of Drug Metabolism

Merck Research Laboratories

a division of Merck & Co.

Inc., Whitehouse Station

USA

[email]@merck.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Drug Metabolism, Merck Research Laboratories, a division of Merck & Co., Inc., Whitehouse Station, USA. 2009
  • Merck & Co., Inc., Whitehouse Station, New Jersey, USA. 2008 - 2009
  • Merck Research Laboratories, West Point, Pennslyvania, USA. 2005

References

  1. Pharmacokinetics of raltegravir in individuals with UGT1A1 polymorphisms. Wenning, L.A., Petry, A.S., Kost, J.T., Jin, B., Breidinger, S.A., DeLepeleire, I., Carlini, E.J., Young, S., Rushmore, T., Wagner, F., Lunde, N.M., Bieberdorf, F., Greenberg, H., Stone, J.A., Wagner, J.A., Iwamoto, M. Clin. Pharmacol. Ther. (2009) [Pubmed]
  2. Effect of rifampin, a potent inducer of drug-metabolizing enzymes, on the pharmacokinetics of raltegravir. Wenning, L.A., Hanley, W.D., Brainard, D.M., Petry, A.S., Ghosh, K., Jin, B., Mangin, E., Marbury, T.C., Berg, J.K., Chodakewitz, J.A., Stone, J.A., Gottesdiener, K.M., Wagner, J.A., Iwamoto, M. Antimicrob. Agents Chemother. (2009) [Pubmed]
  3. Lack of a significant drug interaction between raltegravir and tenofovir. Wenning, L.A., Friedman, E.J., Kost, J.T., Breidinger, S.A., Stek, J.E., Lasseter, K.C., Gottesdiener, K.M., Chen, J., Teppler, H., Wagner, J.A., Stone, J.A., Iwamoto, M. Antimicrob. Agents Chemother. (2008) [Pubmed]
  4. Pharmacokinetics of famotidine in infants. Wenning, L.A., Murphy, M.G., James, L.P., Blumer, J.L., Marshall, J.D., Baier, J., Scheimann, A.O., Panebianco, D.L., Zhong, L., Eisenhandler, R., Yeh, K.C., Kearns, G.L. Clin. Pharmacokinet (2005) [Pubmed]
 
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