¿Usted o alguien que conoce ha tomado Zantac® y posteriormente le han diagnosticado cáncer?
Funcionarios de la Administración de Alimentos y Medicamentos (FDA) han ordenado la retirada inmediata de todos los medicamentos con ranitidina, comercializados bajo la marca Zantac®. Esta orden se debe a la preocupación de que el medicamento pueda contener una sustancia química cancerígena. Según pruebas recientes realizadas por un prestigioso laboratorio independiente y una solicitud presentada ante la FDA, existen afirmaciones de que Zantac® (y la ranitidina genérica) provocan una alta exposición al carcinógeno nitrosodimetilamina (NDMA) en los pacientes. Diversos estudios han relacionado la hepatotoxina NDMA con el cáncer tanto en animales como en humanos.
Aquellas personas que tomaban con frecuencia el medicamento para la acidez estomacal Zantac® y a quienes posteriormente se les diagnosticó cáncer, como cáncer de mama, cáncer de vejiga, cáncer de esófago, cáncer de hígado, cáncer de estómago, cáncer de riñón, cáncer de intestino delgado, cáncer de páncreas, leucemia o linfoma no Hodgkin, podrían tener derecho a presentar una demanda contra los fabricantes y distribuidores del medicamento.
Si usted o un ser querido ha recibido un diagnóstico de cáncer después de tomar este medicamento, evaluaremos su caso sin costo alguno.
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