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1.
Neth J Med ; 63(7): 242-3, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16093573

RESUMO

The case report on cotrimoxazole-induced pancreatitis by Versleijen et al. deals with the assessment of the probability that cotrimoxazole induced the acute pancreatitis: a causality assessment. In this editorial, we comment on this assessment from a clinical, pharmacological and epidemiological perspective. Moreover, the consequences of the results of the assessment are discussed.


Assuntos
Anti-Infecciosos/efeitos adversos , Pancreatite Necrosante Aguda/induzido quimicamente , Combinação Trimetoprima e Sulfametoxazol/efeitos adversos , Humanos , Incidência , Países Baixos/epidemiologia , Pancreatite Necrosante Aguda/epidemiologia
2.
Ned Tijdschr Geneeskd ; 149(26): 1472-4, 2005 Jun 25.
Artigo em Holandês | MEDLINE | ID: mdl-16010961

RESUMO

Two girls, aged 2 and 4 years, with acute gastroenteritis and vomiting, received domperidone and metoclopramide, respectively. Urinary retention developed, but after catheterisation of the bladder was performed once and the medication was withdrawn, both children recovered without further sequelae. Anti-dopaminergic antiemetic agents should be prescribed with caution, especially in young children.


Assuntos
Antieméticos/efeitos adversos , Antagonistas de Dopamina/efeitos adversos , Gastroenterite/tratamento farmacológico , Retenção Urinária/induzido quimicamente , Doença Aguda , Antieméticos/uso terapêutico , Pré-Escolar , Domperidona/efeitos adversos , Domperidona/uso terapêutico , Antagonistas de Dopamina/uso terapêutico , Feminino , Humanos , Metoclopramida/efeitos adversos , Metoclopramida/uso terapêutico
3.
Br J Clin Pharmacol ; 58(3): 326-8, 2004 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-15327593

RESUMO

AIMS AND METHODS: To describe patients with decreased libido during use of a HMG-CoA-reductase-inhibitor, and to discuss causality and pharmacological hypotheses for this association by analysis of the adverse drug reactions (ADR) database of the Netherlands Pharmacovigilance Centre Lareb. RESULTS: Eight patients were identified as having decreased libido during use of statins. In two of these cases testosterone levels were determined and appeared to be decreased. CONCLUSION: Decreased libido is a probable adverse drug reaction of HMG-CoA-reductase-inhibitors and is reversible. The ADR may be caused by low serum testosterone levels, mainly due to intracellular cholesterol depletion.


Assuntos
Ácidos Graxos Monoinsaturados/efeitos adversos , Inibidores de Hidroximetilglutaril-CoA Redutases/efeitos adversos , Hipercolesterolemia/tratamento farmacológico , Indóis/efeitos adversos , Libido/efeitos dos fármacos , Pravastatina/efeitos adversos , Fluvastatina , Humanos , Masculino , Pessoa de Meia-Idade
4.
Br J Clin Pharmacol ; 56(4): 451-2, 2003 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-12968991

RESUMO

AIMS: To investigate the cause of chest pain during the use of bupropion as an aid to stop smoking. METHODS: The Netherlands Pharmacovigilance Centre received 22 reports of chest pain, associated with the use of bupropion as an aid to smoking cessation. Additional information about long-term follow up was collected to analyze whether these complaints herald manifest cardiac disease. RESULTS: All but one patient recovered after withdrawal of bupropion. Seven patients were additionally investigated and in six of them, a cardiac cause could be excluded. During long-term follow-up, no coronary heart diseases were diagnosed. CONCLUSIONS: These reports indicate that chest pain seems to be associated with the use of bupropion, but its origin remains unclear.


Assuntos
Bupropiona/efeitos adversos , Dor no Peito/induzido quimicamente , Inibidores da Captação de Dopamina/efeitos adversos , Abandono do Hábito de Fumar/métodos , Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fatores de Risco
6.
Int J Impot Res ; 15(1): 44-52, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12605240

RESUMO

A total of 76 male patients on renal replacement therapy (RRT) were investigated. Erectile dysfunction (ED) was defined as insufficient erection during visual erotic stimulation (VES) or during sleep as measured with Rigiscan and Erectiometer. Data on medical history, physical examination, and laboratory variables were collected. Furthermore, penile pharmacological duplex ultrasonography (PPDU) was performed. Univariate and multivariate logistic regressions were used to determine prognostic values and to develop prognostic models. Independent prognostic factors for ED were the number of cardiovascular events, waist-hip ratio, body mass index, and acceleration time (AT) as measured with PPDU. Independent prognostic factors for an abnormal AT (>100 ms) were number of cardiovascular events, age category, and the presence of carotid bruits. Independent prognostic factors for insufficient veno-occlusion during PPDU were number of cardiovascular events and supine diastolic blood pressure. The vascular contribution to ED in patients on RRT is substantial. Data from medical history, limited physical examination, and PPDU contribute to the prediction of the vascular contribution to ED.


Assuntos
Disfunção Erétil/diagnóstico , Falência Renal Crônica/complicações , Terapia de Substituição Renal , Adolescente , Adulto , Idoso , Arteriosclerose/complicações , Disfunção Erétil/complicações , Humanos , Falência Renal Crônica/terapia , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Prognóstico , Inquéritos e Questionários
7.
Ned Tijdschr Geneeskd ; 146(41): 1942-4, 2002 Oct 12.
Artigo em Holandês | MEDLINE | ID: mdl-12404911

RESUMO

A 40-year-old woman with a schizoaffective disorder was initially treated with lithium carbonate and haloperidol decanoate, but after three years the lithium was replaced with carbamazepine. Following this, her performance deteriorated over several years despite increasing dosages of haloperidol. After withdrawal of the carbamazepine a remarkable recovery occurred. A pharmacokinetic interaction between haloperidol and carbamazepine, which results in decreased haloperidol blood levels, provides a good explanation of this clinical picture. This clinically relevant interaction should be incorporated into pharmacovigilance systems.


Assuntos
Antimaníacos/efeitos adversos , Antipsicóticos/farmacocinética , Carbamazepina/efeitos adversos , Haloperidol/farmacocinética , Transtornos Psicóticos/tratamento farmacológico , Adulto , Antimaníacos/farmacocinética , Antipsicóticos/efeitos adversos , Carbamazepina/farmacocinética , Interações Medicamentosas , Feminino , Haloperidol/efeitos adversos , Humanos
8.
Br J Clin Pharmacol ; 52(5): 579-86, 2001 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11736867

RESUMO

AIMS: Detection of new adverse drug reactions (ADR) after marketing is often based on a manual review of reports sent to a Spontaneous Reporting System (SRS). Among the many potential signals that are identified, only a limited number are important enough to require further attention. The goal of this study is to gain insight into factors contributing to the selection and dissemination of possible signals originating from the SRS maintained by the Netherlands Pharmacovigilance Foundation. METHODS: In a case control design, all signals (n = 42) disseminated to the Medicines Evaluation Board from the second quarter of 1997 until the third quarter of 2000, which could be expressed as a combination of a single ATC code and a single WHO preferred term, were included. For each case, four controls were matched in time. Logistic regression analysis was used to investigate the influence of various factors, such as the fact whether the ADR or drug is new, the strength of the association, the seriousness of the reaction and the documentation of the reports. RESULTS: Multivariate analysis showed that the presence of a 'serious report' (Odds Ratio 3.8, 95% CI 1.3, 11.0), a WHO 'critical term' (OR 4.7, 95% CI 1.8, 13), the ADR being unlabelled (OR 6.1, 95% CI 2.3, 16) and the presence of a disproportionate association (OR 3.5, 95% CI 1.4, 8) were all independently associated with signal selection. The number of reports and the time after marketing of the drug had no influence. CONCLUSIONS: This study showed that selection of signals is based on both qualitative and quantitative aspects. Knowledge of these factors may improve the efficiency of the underlying signal selection process.


Assuntos
Sistemas de Notificação de Reações Adversas a Medicamentos/estatística & dados numéricos , Sistemas de Notificação de Reações Adversas a Medicamentos/instrumentação , Estudos de Casos e Controles , Interações Medicamentosas , Humanos , Análise Multivariada , Países Baixos , Razão de Chances , Análise de Regressão , Organização Mundial da Saúde
10.
Int J Impot Res ; 13(4): 189-91, 2001 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-11494073

RESUMO

The purpose of this work was to assess whether a single intracavernous injection (ICI) of a low dose of the combination of papaverine-phentolamine is replaceable by a high dose of the oral erectogenic agent sildenafil as mode of stimulation during pharmaco-penile duplex ultrasonography (PPDU). Eleven patients with complaints of erectile dysfunction were included in a crossover study. With an interval of two weeks the patients were exposed to ICI with papaverine/phentolamine (3.75 mg/0.125 mg) and oral administration with sildenafil (100 mg) preceding PPDU. Five patients started with ICI. Six patients started with sildenafil. In the sildenafil stimulation mode, visual erotic stimulation (VES) was used to initiate erection. VES was applied by personal LCD monitor. Cut-off values to define sufficient arterial response were: peak flow velocity (PSV) >25 cm/s and acceleration time (AT) <72 ms. Cut-off value to define sufficient veno-occlusion was a resistance index > or =1.00. Statistical analysis of PPDU parameters shows no significant difference between the two modes of stimulation for arterial response (PSV, AT), whereas the resistance index, as a parameter of veno-occlusive response was significantly higher in the sildenafil mode. This finding is confirmed in the clinical translation of the results: two patients with an insufficient arterial response to ICI had a sufficient arterial response to sildenafil and only one patient showed an insufficient arterial response following sildenafil, whereas the response following ICI was sufficient. Analysis of veno-occlusive responses shows remarkable differences between both modes of stimulation. Whereas following the administration of sildenafil all veno-occlusive responses were classified as sufficient, seven patients showed an insufficient veno-occlusive response following ICI. As mode of stimulation in PPDU, high dose sildenafil yields significantly less false positive diagnoses of 'veno-occlusive dysfunction' than intracavernous injection of the combination papaverine/phentolamine. No difference was found in the quality of the arterial response. Based on this study we conclude that sildenafil may replace ICI as mode of stimulation during PPDU.


Assuntos
Disfunção Erétil/diagnóstico por imagem , Pênis/diagnóstico por imagem , Inibidores de Fosfodiesterase , Piperazinas , Ultrassonografia Doppler Dupla , Administração Oral , Adulto , Idoso , Estudos Cross-Over , Relação Dose-Resposta a Droga , Combinação de Medicamentos , Hemodinâmica , Humanos , Injeções , Masculino , Pessoa de Meia-Idade , Papaverina/administração & dosagem , Pênis/irrigação sanguínea , Fentolamina/administração & dosagem , Inibidores de Fosfodiesterase/administração & dosagem , Estimulação Luminosa , Piperazinas/administração & dosagem , Purinas , Citrato de Sildenafila , Sulfonas , Vasodilatadores/administração & dosagem
13.
Am J Kidney Dis ; 35(5): 845-51, 2000 May.
Artigo em Inglês | MEDLINE | ID: mdl-10793018

RESUMO

The existence of a sexual problem as the subjective evaluation of sexual function was assessed with a simple questionnaire. Those questioned were patients undergoing dialysis treatment (n = 400) or with a functioning renal transplant (RTx; n = 300) and both men and women in the general Dutch population (n = 591). In the Dutch control population, 8.7% of the men and 14.9% of the women reported a sexual problem, showing a significant gender difference but unrelated to age. In patients, the prevalence of a sexual problem was significantly greater (hemodialysis, men, 62.9%; women, 75.0%; peritoneal dialysis, men, 69.8%; women, 66.7%; renal transplantation, men, 48.3%; women, 44.4%). In RTx recipients, sexual problems were significantly less prevalent than in patients undergoing dialysis (P < 0.001). Only in male patients was an association between prevalence of a sexual problem and age found. The results of the simple questionnaire were sufficiently validated when 102 of 104 patients confirmed their responses in a subsequent structured interview. This study shows that the prevalence of sexual problems in patients undergoing renal replacement therapy is high and clinically relevant.


Assuntos
Terapia de Substituição Renal/efeitos adversos , Disfunções Sexuais Fisiológicas/etiologia , Adulto , Idoso , Feminino , Humanos , Entrevistas como Assunto , Masculino , Pessoa de Meia-Idade , Prevalência , Disfunções Sexuais Fisiológicas/epidemiologia , Inquéritos e Questionários
14.
Int Clin Psychopharmacol ; 14(4): 257-8, 1999 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-10468320

RESUMO

A case is presented of painful priapism of the clitoris lasting 3 days, with a strong temporal association with the administration of nefazodone hydrochloride. Priapism has been described as a rare side-effect of drugs with high alpha1-adrenergic blocking potential. However, the alpha1-adrenergic blocking potential of nefazodone is moderate. Drug-induced clitoral priapism has been described for citalopram, bromocriptine, fluoxetine and trazodone combined with fluoxetine. To our knowledge, this is the first report in the literature about priapism of the clitoris associated with nefazodone.


Assuntos
Antidepressivos de Segunda Geração/efeitos adversos , Clitóris/efeitos dos fármacos , Triazóis/efeitos adversos , Doenças Vaginais/induzido quimicamente , Antidepressivos de Segunda Geração/uso terapêutico , Transtorno Depressivo/complicações , Transtorno Depressivo/tratamento farmacológico , Feminino , Humanos , Pessoa de Meia-Idade , Piperazinas , Triazóis/uso terapêutico , Doenças Vaginais/patologia
15.
Pharmacoepidemiol Drug Saf ; 8 Suppl 1: S63-4, 1999 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15073888

RESUMO

The Netherlands Pharmacovigilance Foundation LAREB received five case reports concerning transient impairment of micturition or urinary retention, suspected to be induced by tramadol. In all patients--three women and two men--the symptoms occurred in temporal association with the use of tramadol and promptly recovered after stopping of the drug. Tramadol was taken orally in doses within the recommended therapeutic range (150 mg or less daily). Disturbance of micturition is not mentioned as a side-effect in the summary of product characteristics of Tramal 50 and 100. Tramadol is an opioid agonist, however, and morphine is known to increase the tonus of the bladder sphincter and to cause urinary retention.

19.
Int J Impot Res ; 8(2): 59-62, 1996 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-8858391

RESUMO

Erectile response to intracavernous pharmacological stimulation is highly susceptible to stress and anxiety provoked by the test-situation. To reduce false-positive diagnosis of veno-occlusive dysfunction and to limit the need for high-dosage pharmacotesting, we developed the Post-Investigation Questionnaire (PIQ-R), a self-report instrument to assess erectile response to pharmacological stimulation after the patient has left the office. In this study veno-occlusive sufficiency was not demonstrated in 80 of 105 patients with erectile dysfunction at the time of pharmaco-penile duplex ultrasonography. PIQ-R detected sufficient erectile response in 40 of these patients, thus reducing false-positive diagnosis of veno-occlusive dysfunction by 50%. We also found that reports of sexual activity after investigation increased interest in auto-injection therapy. PIQ-R is a practical self-report measure to assess erectile response after clinical pharmacotesting, and to more carefully select patients for auto-injection therapy.


Assuntos
Disfunção Erétil/tratamento farmacológico , Disfunção Erétil/fisiopatologia , Papaverina/administração & dosagem , Ereção Peniana/efeitos dos fármacos , Inquéritos e Questionários , Vasodilatadores/administração & dosagem , Disfunção Erétil/diagnóstico por imagem , Reações Falso-Positivas , Humanos , Impotência Vasculogênica/diagnóstico por imagem , Injeções , Masculino , Pessoa de Meia-Idade , Papaverina/uso terapêutico , Pênis/diagnóstico por imagem , Comportamento Sexual/efeitos dos fármacos , Ultrassonografia , Vasodilatadores/uso terapêutico
20.
Urol Clin North Am ; 22(4): 803-19, 1995 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-7483130

RESUMO

To date, several accurate tests for diagnosing vascular ED may be chosen. It is necessary to be well aware of the purpose of testing: global assessment of erectile capacity in preparation for auto-injection therapy, or detailed assessment of arterial and erectile response in preparation for surgical treatment. Pharmacotesting may be sufficient for the majority of patients. Other, more invasive tests are reserved for preparing surgical treatment or scientific studies.


Assuntos
Impotência Vasculogênica/diagnóstico , Humanos , Impotência Vasculogênica/fisiopatologia , Masculino , Ereção Peniana/efeitos dos fármacos , Ereção Peniana/fisiologia , Pênis/diagnóstico por imagem , Pênis/efeitos dos fármacos , Pênis/fisiologia , Radiografia , Cintilografia , Ultrassonografia Doppler/instrumentação , Ultrassonografia Doppler/métodos
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