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Post Info TOPIC: side effects


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RE: side effects
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I've also had (work-related?) mild tinnitus for a number of years. Pretty sure it's a bit louder or more perceptible at times on Harvoni. I'm not finding it to be very intense or difficult to tolerate though. Hopefully it will diminish after the treatment's end.

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61 yo, GT 1a, liver F1-F2 pre-treatment.

Diagnosis circa 2000. tx naive till 8/6/15, Harvoni tx initiated 8/6/15 through Gilead's Support Path. 28day labs: virus "und." Sides mild. EOT 10/28/15. EOT liver enzymes normal range: AST 25, ALT 18.



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What did you say Judy?  I can't hear you.  I have this LOUD screeching in my ears.  :)         I had this before tx so I really can't say if it was exacerbated by the Harvoni.  As Tig said there have been a few members mention this as a side effect of tx.  I need to turn the music up. :)



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1b  Int/Riba relapse @ 48 weeks.  Stop tx Peg Int/Riba 12 weeks ill. Relapse S/O 6/23/14 :(   Started Harvoni 11/12/14  EOT 4/28/15.  EOT+4 UND :)  SVR! 8/4/15  :)     Thankful for every morning.

Tig


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Hi, 

Yep, there have been several people mention the onset of "Tinnitus" during/following Harvoni treatment. I developed  it from another protocol and it is awful! I haven't heard anyone mention it persisting after Harvoni treatment, but I'm sure your fellow warriors will chime in. I find it very annoying at night and have to use a noise generator to help mask it some nights. You can find free apps for your phone that help.



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Tig

68yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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Well it has been two weeks since I started taking Harvoni. Doing okay as far as minimal side effects but I am really being bothered by this loud constant ringing in my ears. Just wondering if anyone else has experienced this.



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Judy

72 yo. Diagnosed 2002 genotype 1.  IV Heroin user 1960's-70's. V/L 5945743. 2005 interferon/ribavirin 48 wks, relapsed. Started Harvoni 9/11/2015.

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