P. Veyssier

Publication List Details

Period

1990 - 1993

Number

6

Co-Authors

A non-comparative, multicentre study of cefepime in the treatment of serious bacterial infections (1993)

Mouton, Y., Chidiac, C., Humbert, G., Leroy, J., Veyssier, P., Modai, J., ...

Multi-resistant strains of Gram-negative bacteria are rapidly emerging as a frequent cause of serious bacterial infection in the hospital environment. Effective treatment must include an antibiotic...

A non-comparative study of the efficacy and tolerance of cefepime in combination with amikacin in the treatment of severe infections in patients in intensive care (1993)

Gouin, F., Papazian, L., Martin, C., Albanese, J., Durbec, O., Domart, Y., ...

Patients in intensive care units (ICUs) are at increased risk of developing nosocomial infections. This is of special concern in the immunocompromised patient, particularly with regard to...

Pharmacokinetics of cefodizime in elderly patients with moderate or severe renal impairment (1990)

Veyssier, P., Devillers, A., Domart, Y., Fourtillan, J. B., Bryskier, A., Procyk, T.

In young adults, the elimination half-life of cefodizime is 3.5–4 h. A pharmacokinetic study was performed in eight patients, aged 63 to 85 years, divided into two groups with the following...

Safety, pharmacokinetics, and antiviral activity of A77003, a C2 symmetry-based human immunodeficiency virus protease inhibitor.

Reedijk, M, Boucher, C A, Van Bommel, T, Ho, D D, Tzeng, T B, Sereni, D, ...

A77003, an inhibitor of the human immunodeficiency virus type 1 (HIV-1) protease, was administered to asymptomatic HIV-1-infected patients in a phase I trial. The drug was given by continuous...

Safety, pharmacokinetics, and antiviral activity of A77003, a C2 symmetry-based human immunodeficiency virus protease inhibitor.

Reedijk, M, Boucher, C A, Van Bommel, T, Ho, D D, Tzeng, T B, Sereni, D, ...

A77003, an inhibitor of the human immunodeficiency virus type 1 (HIV-1) protease, was administered to asymptomatic HIV-1-infected patients in a phase I trial. The drug was given by continuous...