Zobrazeno 1 - 10
of 104
pro vyhledávání: '"C. Kreft-Jais"'
Publikováno v:
British Journal of Dermatology. 166:1333-1341
Summary Background The question of quantitative and qualitative differences between adverse drug reactions (ADRs) to tetracyclines was raised many years ago, especially for minocycline and doxycycline. Objectives To assess and compare ADRs related to
Autor:
Evelyne Jacqz-Aigrain, Véronique Lamarque, E. Autret-Leca, L. Becquemont, M.-J. Boutroy, P. Carlier, A. Castot, C. Cornu, C. Damase-Michel, J.-P. Demarez, E. Dohin, M. Gersberg, C. Kreft-Jais, H. Le Louet, F. Meillier, J.-L. Parier, G. Pons, D. Subtil, T. Vial
Publikováno v:
Therapies. 61:297-304
Data required to asses the risk of a new drug regarding the normal course of pregnancy as well as embryo, fetal and neonate development, are often missing when a new product is launched. In such a situation, a risk management plan is to be developed
Autor:
Evelyne Jacqz-Aigrain, Véronique Lamarque, E. Autret-Leca, L. Becquemont, M.-J. Boutroy, P. Carlier, A. Castot, C. Cornu, C. Damase-Michel, J.-P. Demarez, E. Dohin, M. Gersberg, C. Kreft-Jais, H. Le Louet, F. Meillier, J.-L. Parier, G. Pons, D. Subtil, T. Vial
Publikováno v:
Therapies. 61:287-295
Resume Les donnees evaluant le risque d’un nouveau produit sur le deroulement normal de la grossesse et le developpement de l’embryon, du fœtus et du nouveau-ne sont le plus souvent manquantes lors de la mise sur le marche d’un nouveau produit
Autor:
F. J. De Abajo, Dolores Montero, C. Kreft-Jais, R. Coulson, J. L. Monteagudo, Nicholas Moore, A. Biron
Publikováno v:
Pharmacoepidemiology & Drug Safety. 3:157-162
The development of telematic exchange of information in pharmacovigilance has as a consequence the necessary development of the messages used to transmit the information. The first of these messages is the one used to transmit information on individu
Autor:
R. Palop, C. Kreft-Jais, F. J. De Abajo, A. Biron, R. Coulson, Nicholas Moore, Dolores Montero
Publikováno v:
Pharmacoepidemiology & Drug Safety. 3:151-155
Pharmacovigilance is a field where communication is paramount. Information, such as single case reports, is transferred from health professionals to National Regulatory Administrations and between administrations and industry. The cumulation of repor
Autor:
K. Wigglesworth, Dolores Montero, J. L. Monteagudo, C. Kreft-Jais, F. J. De Abajo, A. Biron, R. Coulson, Nicholas Moore, J. L. Zabala
Publikováno v:
Pharmacoepidemiology & Drug Safety. 3:163-167
Publikováno v:
Therapie. 57(3)
The academic interest for pharmacovigilance appears to be very low, because of the judged weakness of a "significant" relationship between drug utilisation and pathological events. We have tried to collect the relevant surveys of the French pharmacov
Publikováno v:
Therapie. 50(6)
The French drug surveillance (pharmacovigilance) system is based on a network of 31 regional centres which receive adverse drug reaction (ADR) reports from health professionals and are drug information centers. Cases are entered into a common databas
Publikováno v:
Therapie.
The pharmacological class of calcium channel antagonists (CCA) is, with beta-adrenergic antagonists, diuretics, converting enzyme inhibitors and alpha-adrenergic antagonists, one of the first line monotherapies of essential hypertension, according to
Publikováno v:
La Revue du praticien. 42(20)
Novel angiotensin converting enzyme inhibitors (ACE inhibitors) have recently been commercialized and the question arises whether differences in pharmacodynamic and pharmacokinetic properties should lead to specific therapeutic choices. To our knowle