Epclusa Side Effects (Page 8)
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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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Re: Lou (# 15)

The anxiety is unbearable I am a shell of who I use to be I had no liver damage and was living a wonderful life we were not told the truth about this drug my life is destroyed Please join Harvoni Epclusa post you can search it anywhere it will come up can’t drive a car anymore or even live peacefully the drug was pushed through to fast. And we were the lab rats I have lost vision in my eye have cataracts severe floaters and my muscles spasm all the time.

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Re: New day (# 14)

Agree totally,I felt ok pre treatment,now it's 14 mths Poste treatment iv so many problems now numb feet hands swollen abdomen arthritis nausea anxiety just too many problems ,hate to think what's next,the liver clinic that scared me into doing treatment no support at all,in fact Iv had the misfortune of having suffer a lot of poor excuses over my yrs but IV never had anybody destroy my life like the Epclusa people ,not even a oh we are sorry about what our new wonder med has done to you.think the DAAs keep working on destroying things in your body long after the virus has gone ,I'm sitting here 4am Thurs morning after being awake all night looking at my puffed out deformed looking feet,anyway good luck hope people have better luck,,peace,

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Re: VerFree (# 2)

So you work for the pharmaceutical company?
Many of us were symptom free for 35 yrs. had these Anti virals pushed on us and life was never the same. There is more in these drugs then anti virals
Until it’s you, comment many of our lives have been cut in half post treatment. By ny virus or hello death?

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Re: VerFree (# 2)

I call BS. Just like Harvoni this drug is making people sick, sicker and killing others. My husband had NO CANCER in his blood work or scan. Started drug and died 5 months to the day of start treatment date ... liver, pancreas and adrenal glands. Follow the patients after treatment.

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Re: Lou (# 11)

Hi Lou it seems the miracle was not a miracle drug after all. It was pushed through too fast not enough time to see the side effects they are devastating unbearable. Harvoni and Epclusa posts have so many people in the same situation. I have gone to Drs for 4 years had every test and scans and feel something happened to my immune system and I am in overdrive.

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Re: Friendz4 (# 9)

Sounds very similar to me. My breathing seems to be getting worse. What kind of breathing problems are you getting? So sick of bloating and body jerks, it's like the treatment has effected everything. I felt so much better before I touched Epclusa. Anyway please take care, we are not alone.

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Re: VerFree (# 2)

I.m also having restless leg body jerks every day also really bloated around stomach ,but I haven't gained much weight also ,I'm worried they say virus is cured ,but I have definitely got liver symptoms happening,the liver people who signed me up are no help at all , favourite line is damage was probably done years ago would not be the DAAs ,I'm forever dropping coffee cups due to numbness feet puffy toes look puffy anxiety there's heaps I could go on for ages,I tell my GP all he says is oh I spoke to liver clinic they said treatment wouldn't do this ,mmm it all seems to much for him,I had abdominal xray yesterday I wonder what or if it finds anything ,I'm 66yrs old I was Geno 3also VL very high before tx .cheers take care

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Re: Lou (# 5)

These side effects were not mentioned prior to treatment if they had been I would not have taken this treatment I have severe tinnitus 24/7 hearing loss. My head is always clogged up, neuropathy through my body. Hands and feet are the worst. Extreme anxiety, awful brain fog, and confusion rashes that never went away since treatment. My Immune system is so messed up I have muscle spasms, and something happened to sleep pattern, breathing problems and I have been to Drs for 4 years during treatment. My Dr said like all of you it’s not from the treatment. Well it’s not a coincidence that these side effects are the same we are all experiencing. {edited for privacy}

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Re: Lou (# 7)

Hi Lou we are on a group of people harmed severely from these DAA with no support from Dr they all say the same thing it’s not from the med it is not a coincidence that all these same side effects are happening to us. {edited for privacy}

Editor's note: Per our privacy policy, personal contact information (such as telephone numbers, email addresses, etc) is not allowed to appear on our discussion threads.

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Re: VerFree (# 2)

It's more than a coincidence ,that so many people have gotten sick, shortly after starting Epclusa DAAs don't you think, IV heard too many times from ignorant people that they have never heard of that symptom before ,and try to blame it on something else ,when is somebody going to aim up ,and admit that very little was known about the wonder med ,let's find a minority group of guinea pigs and make some $$$

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Re: Lou (# 3)

I am a 54 yr old female. This is my second round of treatment for Hep C. The first involved shots in the stomach once a week and two pills daily. That was a nightmare hair loss, restless leg syndrome, vomiting, weakness, similar to chemo. But I understood sometimes it takes a poison to kill one. Now my Hep C has returned. Just started Epclusa and I have to take it when I come home from work. It puts me in a deep sleep. So deep that if the house was on fire I wouldn't wake up. Also I get strange heartburn even without eating. I feel bloated but my scale says different. I have someone at home when I take it so nothing happens while I'm sleeping. But that is it. These issues are nothing compared to the last time. And 12 weeks is nothing compared to a year. I am sorry to hear that you are having a these issues.

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Hi Kathleen, hope you are doing ok. We've still got fires and smokey air, not much fun with breathing problems. My breathing problems don't seem to be responding to the cortasteroids; just bloated and exhausted as usual. Now I've got a letter telling me I have an appointment for a stress test on Monday on a treadmill. Not looking forward to it much, as I seem to have a lot of symptoms that go with heart problems. If that's what it is there's not much I can do about it. I still feel Epclusa has caused my problems. They will never admit it. The thought of going on treadmill scares me, as I haven't had much energy as of late with the bad air I've been breathing. It's been near 3 months now. Sick of it now. I feel I've just about had enough of doing tests, paying out money and getting nowhere. Hope you're ok. Sorry for the whining, bad day today.

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Re: VerFree (# 2)

I think it's not a coincidence that a lot of people have lived near normal lives untill post treatment ,my virus has gone thankfully but so has my pain free days ,ears constantly ringing nausea total exhaustion numbness severe joint pain Edema infections ect .but oh I forgot very few side effects, sure thing mmm.

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Re: VerFree (# 2)

I'd like to see the percentage of people over 40yrs old who have done treatment who now have major health problems some fatal instead of being fed rubbish about very few sideeffect s ,I think that there would be a lot of people who would have not done treatment ,and took there chance with hcv instead of living in severe pain every day ,knowing that there's no body out there with a clue with what is going on with our bodies or any idea what damage the DAAs have done or what they will do , Also no support from the people who convinced us to do treatment ,I think it's about time some people looked up Epclusa post treatment side effects .

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I am very sorry that you've both been miserable, I know it is very frustrating. The issue, however, is that the virus can be fatal, so the issues caused by the treatments have to be carefully weight against potential death.

Epclusa has been known to cause side effects, such as anemia, weakness, unusual tiredness, trouble sleeping, cough, and depression.

Issues similar to what you've both described have been reported, but it is hard to say if they are from the virus, the treatment, a combination of both, and/or how long they last after treatment.

Is there anything I can help with?

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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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