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1.
Melanoma Res ; 31(1): 88-91, 2021 02 01.
Artigo em Inglês | MEDLINE | ID: mdl-33234847

RESUMO

Nowadays, anti-programmed death-1 (PD-1) antibodies are the first-line treatment for metastatic malignant melanoma. An infusion reaction is an adverse event that could occur due to monoclonal antibodies administration and requires prompt diagnosis and treatment. In this article, we report on a case of stage IV malignant melanoma treated with nivolumab, in which a severe infusion reaction occurred, manifesting as flushing and hypotension followed by bronchospasm. The switch to pembrolizumab was both a well-tolerated and effective therapeutic alternative.


Assuntos
Antineoplásicos Imunológicos/efeitos adversos , Melanoma/tratamento farmacológico , Nivolumabe/efeitos adversos , Humanos , Masculino , Melanoma/complicações , Pessoa de Meia-Idade
2.
Curr Eye Res ; 41(7): 890-6, 2016 07.
Artigo em Inglês | MEDLINE | ID: mdl-26554729

RESUMO

PURPOSE: Tacrolimus ocular preparations are commonly employed in autoimmune or inflammatory ocular disorders. However, currently there are not yet approved ocular formulations. Tacrolimus ocular side effects have been reported in clinical use, so the evaluation of different pharmaceutical preparations is mandatory. In this study, the local corneal tolerance and safety profile of three common tacrolimus 0.03% pharmaceutical preparations were evaluated. MATERIAL AND METHODS: Corneal irritation and permeability of tacrolimus preparations were evaluated with the bovine corneal opacity and permeability (BCOP) test. Complementary corneal hematoxylin/eosin and immunohistochemistry staining for tight junctions and adherent junctions E-cadherin, VE-cadherin and zonula occludens-1 were examined and scored to evaluate and to confirm corneal disruption and irritation scores obtained with the BCOP method. RESULTS: Commercial brand ointment (Protopic®), topical compounded eye ointment (pharmacy elaboration) and tacrolimus suspension eye drops (elaborated from parenteral prograf®) were tested as potential ocular preparations to be used in clinics. Tacrolimus preparations hereby studied do not alter the opacity and permeability of the bovine cornea by more than three units, measured by the In Vitro Irritancy Score, neither affected the immunohistochemical parameters, composite score or transepithelial electrical resistance. CONCLUSIONS: Tacrolimus preparations studied can be safely applied as a topical ocular treatment.


Assuntos
Córnea/metabolismo , Opacidade da Córnea/tratamento farmacológico , Tacrolimo/administração & dosagem , Animais , Bovinos , Córnea/efeitos dos fármacos , Opacidade da Córnea/induzido quimicamente , Opacidade da Córnea/metabolismo , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Imuno-Histoquímica , Imunossupressores/administração & dosagem , Irritantes/toxicidade , Soluções Oftálmicas/administração & dosagem , Soluções Oftálmicas/farmacocinética , Permeabilidade/efeitos dos fármacos , Tacrolimo/farmacocinética
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