Pacientes que usam o remédio, mesmo nos lotes afetados, devem continuar o uso. Recolhimento é preventivo.
A Agência Nacional de Vigilância Sanitária (Anvisa) determinou, nesta quinta-feira (23), o recolhimento e interdição de diversos lotes de vários fabricantes do medicamento losartana, usado para tratar pressão alta.
A agência recomendou que os pacientes que usam o remédio, mesmo que ele esteja entre os lotes afetados, devem continuar o tratamento, pois a medida é preventiva.
Em caso de dúvida ou se precisar de orientação, o paciente deve conversar seu médico.
“A hipertensão e insuficiência cardíaca exigem acompanhamento constante e qualquer alteração no tratamento deve ser feita somente pelo médico que acompanha o paciente. Deixar de tomar o medicamento pode trazer riscos para a saúde do paciente”, reforçou a Anvisa.
A Anvisa orienta que você continue o tratamento e converse com o seu médico se precisar de orientações, mesmo que seu medicamento esteja entre os lotes.
É importante que você não pare o tratamento. Só troque de remédio quando já tiver uma nova caixa em mãos, pois parar o remédio pode trazer problemas imediatos à saúde – como derrame, ataques cardíacos e piora da insuficiência cardíaca, inclusive com risco de morte.
A lista é extensa e inclui remédios dos laboratórios: Aché, Biolab Sanus, Brainfarma, Cimed, Eurofarma, Geolab, Teuto e Prati, Donaduzzi & Cia. Confira a lista clicando aqui
Você pode conferir o fabricante e o número do lote do seu medicamento na lista abaixo:
/i.s3.glbimg.com/v1/AUTH_59edd422c0c84a879bd37670ae4f538a/internal_photos/bs/2022/a/9/8luIUIRkGO9yRuetIsvQ/lotes-losartana-interditados.png)
Lista de lotes do medicamento Losartana interditados pela Anvisa em 23/06/22 — Foto: Reprodução
Depois de falar com o seu médico, se for trocar o medicamento, você deve entrar em contato com o Serviço de Atendimento ao Consumidor (SAC) do laboratório que fabrica a sua losartana para se informar sobre a troca.
O contato das empresas aparece na embalagem e na bula do remédio. É dever da empresa fazer a substituição ou a troca do remédio – os lotes que foram mantidos no mercado são considerados seguros e podem ser consumidos.
A agência detectou a impureza “azido” – uma substância que pode causar mutações – em uma concentração acima do limite de segurança aceitável nos remédios. A medida é preventiva.
A presença do azido no insumo farmacêutico da losartana foi identificado no mundo em setembro de 2021. O contaminante pode aparecer durante a produção do insumo farmacêutico ativo, que é utilizado pela indústria farmacêutica para fabricar o medicamento final.
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