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1.
Rev Med Suisse ; 2(61): 976-80, 2006 Apr 12.
Artigo em Francês | MEDLINE | ID: mdl-16686330

RESUMO

Overtreatment (unnecessary treatment, excessive drug dosages, unjustified polypharmacy) alters the risk-benefit ratio. Its prevention requires the recognition of the situations and the understanding of the mechanisms leading to it. The pharmacological treatment of epilepsy exposes to such a risk and serves as an example for its detection and correction.


Assuntos
Anticonvulsivantes , Epilepsia/tratamento farmacológico , Quimioterapia Combinada , Uso de Medicamentos/estatística & dados numéricos , Feminino , Humanos , Risco
2.
Ann Pharm Fr ; 64(3): 161-72, 2006 May.
Artigo em Francês | MEDLINE | ID: mdl-16710114

RESUMO

Two retrospective epidemiologic studies have shown that cannabis is the main psychoactive substance detected in the blood of drivers suspected of driving under the influence of psychotropic drugs. An oral administration double-blind crossover study was carried out with eight healthy male subjects, aged 22 to 30 years, all occasional cannabis smokers. Three treatments and one placebo were administered to all participants at a two week interval: 20 mg dronabinol, 16.5 mg D9-tétrahydrocannabinol (THC) and 45.7 mg THC as a cannabis milk decoction. Participants were asked to report the subjective drug effects and their willingness to drive under various circumstances on a visual analog scale. Clinical observations, a psychomotor test and a tracking test on a driving simulator were also carried out. Compared to cannabis smoking, THC, 11-OH-THC and THC-COOH blood concentrations remained low through the whole study (<13.1 ng THC/mL,<24.7 ng 11-OH-THC/mL and<99.9 ng THC-COOH/mL). Two subjects experienced deep anxiety symptoms suggesting that this unwanted side-effect may occur when driving under the influence of cannabis or when driving and smoking a joint. No clear association could be found between these adverse reactions and a susceptibility gene to propensity to anxiety and psychotic symptoms (genetic polymorphism of the catechol-O-methyltransferase). The questionnaires have shown that the willingness to drive was lower when the drivers were assigned an insignificant task and was higher when the mission was of crucial importance. The subjects were aware of the effects of cannabis and their performances on the road sign and tracking test were greatly impaired, especially after ingestion of the strongest dose. The Cannabis Influence Factor (CIF) which relies on the molar ratio of active and inactive cannabinoids in blood provided a good estimate of the fitness to drive.


Assuntos
Condução de Veículo , Cannabis/efeitos adversos , Dronabinol/efeitos adversos , Alucinógenos/efeitos adversos , Adulto , Método Duplo-Cego , Humanos , Masculino , Desempenho Psicomotor/efeitos dos fármacos
3.
J Neuroimmunol ; 99(1): 131-41, 1999 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-10496186

RESUMO

Interferon-beta regimens for immune-mediated diseases, such as multiple sclerosis (MS), have not been compared regarding their biological effects. In this randomized, parallel-group, placebo-controlled study, cytokine secretion by mitogen-stimulated PBMCs and serum response markers were assessed in volunteers receiving subcutaneous recombinant IFN beta-1a (Rebif, Ares-Serono) 22 microg once a week (QW), 22 microg three times a week, 66 microg QW, or placebo. The production of IL-1beta, IL-6, IFN-gamma, TNF-alpha and TNF-beta markedly decreased during 24-48 h after each injection, with limited dose-dependency and no evidence of tolerance or effect augmentation over 1 month. IL-10 secretion remained unchanged. The increase in serum beta2-microglobulin, neopterin and 2-5A-synthetase was more sustained. Thus, IFN-beta-induced immunomodulation in vivo strongly depends on the administration schedule, the time-integrated effect being 2-3 times greater when a same weekly dose is divided in three injections.


Assuntos
Fatores Imunológicos/administração & dosagem , Interferon beta/administração & dosagem , Ativação Linfocitária/efeitos dos fármacos , Linfocinas/metabolismo , Linfócitos T/metabolismo , 2',5'-Oligoadenilato Sintetase/sangue , Adulto , Relação Dose-Resposta Imunológica , Esquema de Medicação , Fadiga/induzido quimicamente , Febre/induzido quimicamente , Cefaleia/induzido quimicamente , Humanos , Fatores Imunológicos/efeitos adversos , Fatores Imunológicos/uso terapêutico , Interferon beta-1a , Interferon beta/efeitos adversos , Interferon beta/uso terapêutico , Interferon gama/metabolismo , Interleucina-1/metabolismo , Interleucina-6/metabolismo , Linfotoxina-alfa/metabolismo , Masculino , Neopterina/sangue , Proteínas Recombinantes/administração & dosagem , Proteínas Recombinantes/efeitos adversos , Proteínas Recombinantes/uso terapêutico , Segurança , Linfócitos T/efeitos dos fármacos , Fator de Necrose Tumoral alfa/metabolismo , Microglobulina beta-2/análise
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