Epclusa Side Effects (Page 9)
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Hello. I am 16 months post epclusa and feel worse than when I started. I was a server for over 40 years. Full of energy. Then hep c happened. I had epclysa for 12 weeks. Now I am in bed most of the tune from no energy. My ears are ringing. I feel deflated. Anyone else feel like this? My hep c nurse waived off my complaints.

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Hi Kathleen, I really feel for you, I finished Epclusa a year ago and like you I've had so many side effects l can hardly walk most afternoons due to leg joint pain. I get exhausted so easily, nausea, numb toes/fingers; probably a circulation problem. I did not have any of these problems pre-treatment. I've also got Edema on my legs and my stomach is really swollen. I feel so uncomfortable and unbalanced. If I mention this to the hep C liver people they just say, "oh it wouldn't be the treatment". So far the virus isn't showing, but I think I'd rather have the virus then feel like this. All I hear from the liver people are lies, plus no support when I ring them. I'm in Australia. I feel like a guinea pig and my life is wrecked. I think there is going to be a lot of very sick people in the near future. They know nothing about what DAAs do in a couple years time. Really hope you are ok. Take care.

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