I would like to discuss my Viread "side effects" with you. But first some relevant data.
Got diagnosed with Chronic Hep B in March 2011:
- Hbeag Negative
- Genotype D
- Grading 0-1
Started Viread (Tenofovir) in April:
- HBV DNA in April: 29.000
- HBV DNA in May: 45
- HBV DNA in August: Undetectable
- Hbsag in August: 30.000 (First time it got measured.)
So far so good, but here comes the "strange" data:
- ALT in April and before: Between 65 and 73
- ALT in May after I started Viread: 93
- ALT in August: 93
Besides I have some "side effects" since I have been taking Viread that one could sum up as the typical symptoms of acute hepatitis b OR the side effects under Interferon:
- Pain over the location of the liver (on the right side of the abdomen, under the lower rib cage). I never experienced that before taking Viread
- Flu like symptoms: Muscle aches; Headache, Temperature, Tiredness. They come and go. Again I did not experience that before.
My doctor says this COULD be some immune reaction but wants to wait for the next results in November. Because she was also a bit surprised by the rise of my ALT since she figured it should have rather dropped considering the decrease of my HBV DNA.
Any ideas out there? Anyone who experienced something like that in therapy? Would be glad to hear your thoughts and opinions. And thanks for this community here!
I also started on Viread in March 2011. Before taking Viread i had absolutely no symptoms. Upon resuming viread i started experiencing the same symptoms as you have. I checked out the viread site to see if these symptoms were normal and from what i read they seemed to be quite usual and covered in the broad range of possible symptoms experienced by patients while taking viread.
However i would like to hear any contrary opinions if anyone has any.
Even though this might sound "naive" the "side effects" I mentioned do not "feel" like they were caused by the pills directly. If that makes any sense at all. It rather "feels" that there is something going on in my body hepatitis wise, which would explain the risen ALT.....Of course, they also do kind of fit into this very broad range of symtoms mentioned on viread.com. But it just does not feel like sides caused by some pills.
Severe liver problems: Severe liver problems can happen in people who take VIREAD or similar medicines. In some cases these liver problems can lead to death. Your liver may become large (hepatomegaly) and you may develop fat in your liver (steatosis) when you take VIREAD. Call your healthcare provider right away if you have any of the following symptoms of liver problems: Your skin or the white part of your eyes turn yellow (jaundice), dark “tea-colored” urine, light-colored bowl movements, loss of appetite for several days or longer, nausea, stomach pain.
Just as a precaution, I believe you should get your liver checked with an ultrasound or any necessary test to ensure your liver is OK. It is not normal to feel pain. I personally didn't have any of these symptoms and my ALT went from 32 to 21. I hope it is an immune reaction that will cause your virus to be cleared but you can not just wait and risk the worst.
I started Viread therapy in August as a continuation of Entecavir therapy (a long story...). On 1. of August i just switched from Entecavir to Viread. One week later i woke up with a mild skin rush on my abdomen area, i had nausea after taking tenofovir( at the evening) an in the morning and i had also 4 days long fever about 39°C....and i´m PERMANENT tired:o(
Before starting Viread my ALT was 95 and two weeks later 113. I read somewhere that an elevated ALT count is normal after starting nucs (only the first few months), but I´m not sure, i hope that someone with more kowledges will read this to affirm it!
Now, more than a month after starting viread, i feel good( i have only nausea from time to time) and i pray for a negative PCR(the last one before taking Viread was 116).
I hope that the side effects that you experience will disappear soon!!!
Nope, I do not have any other infection. In fact my high ALT was the only abnormal result of my last blood test. Everything else was fine. If I am clearing I would be more than happy. However, I do not want to put too much hope in it because from what I have read this would come close to winning the lottery. But then, someones gotta win it ;)
About my doctor, I do not want to put her into a bad light because she is really competent. She also mentioned that it could be a immune reaction and that she had some rare cases of people clearing it within a year. But I guess she did not want put any false hope in me at the moment. Even though she mentioned there is a chance of clearing considering the count of my hsbag. Anyway, she made it clear that we have to await the results in November...
@Izzy79: I only heard about the rise of ALT in therapy under Interferon so far. But maybe it also happens under nucs. Anyway, all the best for you and keep us informed. The negative PCR will come ;)
@all: Thanks for the discussion. It sure feels good to talk to people fighting the same fight!!!
Since I am new to the topic is my count of hbsag high and therefore good? But I am not hbeag positive I am negative. Speaking of, what I still do not clearly understand because of all the misleading information in the internet. At the end of the day, is it good or bad if your body got rid of the hbeag?
so, in my opinion the ALT increase is not do to the Viread, actualy Viread stop the increase (or it was only a coincidence).
65 in May, 73 in March -> a increase without Viread in one month
73 in march -> 93 in may -> a increase but posible not to viread (we have 2 mouth )
93 in may -> 93 in August -> same level under Viread (2 mounth), no increase, so we can say that viread some how stop the increase.
maybe is to mathematical, but also this option desired to be mentioned
I only checked before i started taking viread. At that time my doctor said my liver was perfectly normal. Before i started taking Viread:HBsAG : Positive
Viral DNA=00/ Undetectable
Liver function: Very Good
Hep B Core Antibody: Positive
Anti HBe (igM): Negative
Anti HBe (igG) (H): Positive. So my doctor suggested i take Viread for a year to make sure everything was under control.
Since resuming taking Viread in March and heavily dozing on fruits, taking vit B, C and D supplements i started having tired spells, which mostly happen early in the mornings and late evenings. At those times i was also taking Chanca Piedra tea and was taking daily detox pills. So i decided to stop taking the teas and stopped the detox pills too leaving only the Viread and fruits. Infact at a point getting out of bed in the morning became a problem, cos i'd be feeling absolutely wasted. I ran back to my doctor who said the symptons were normal and showed that the infection was clearing. He sounded so optimistic that we would achieve complete viral suppression by March 2012.
Months down the line up till this moment i feel great. I still feel a bit of sensitivity to the right side of my abdomen and occasional flu like symptons which come and go but all else is absolutely fine. Also i kind of feel my energy level was more before i started taking viread. But i am happy knowing that this is due to the fact that my immune system is fighting and clearing. I also plan to introduce Alinia soon.
@ all: Thanks all for all the encouragements and support. I love you all to bits!!!!
Yes i got to find out the same thing. My Doctor was being overly too careful. He should never have prescribed Viread. Anyway, He said he will discontinue the viread for me in 6 months, but i also have to think of the best way to stop taking it safely. My Plan: Comboing Interferon with Alinia and then taking off the viread gradually.
wow, indeed it was overly too careful or I don't know. I try to think on what he wanted to achieve, because all the doctors that prescribe nucs, they target viral load undetectable, but you already have this.
anyway, is to late to debate on this and as far as I read, your plan sound like a good plan to me, and I think that @Stef 2011 can advise you in more details.
bwt, do you check your AgHBs quantitative ?
Good luck on your plan and if is posible keep us posted with the implementation and results.
Yes i got to find out the same thing. My Doctor was being overly too careful. He should never have prescribed Viread. Actually to be fair to him, When i told him after a month that i wasn't too comfortable taking viread as i was having a bit o f insomnia at the time, he was going to take it off, as he told me: "You dont need it. I only prescribed it just to be doubly sure we have everything under control". I then opted to continue it if it was going to have any benefits for me in any way. i was desperate at the time. Had just been told my HBsag was positive and i was pretty scared and desperate to do anything to assure my self i was going to be fine! Anyway, on my last visit, He said he will discontinue the viread for me in 6 months from now, but i also have to think of the best way to stop taking it safely. My Plan: Comboing Interferon with Alinia and then taking off the viread gradually.
@ 4est: Many Thanks. I actually have never checked my AgHBs quantitative. But i plan to do both AgHBs and AbHBs as soon as possible to track clearance. Will keep you all updated on implementation and results. Thanks again.
@enolia: Got the ultrasound. Liver does not look abnormal. But for the bloodtest I will have to wait until November...
@all: One more question. Before I found out that I have chronic hepatitis in March 2011. I got vaccinated in 1998 (triple shot) and again in 2009 (one shot). So they say to be protected against HBV you need a titer >100. When the chronic Hep B got diagnosed I had a titer of 10. Finally the question: Does that mean that my immune system once reacted against HBV? Is that count valuable for anything: prognosis for therapy, date when I might have been infected (my doctor thinks before my first shots in 1998 but why do I have a bit of a titerthen?). Maybe someone here knows about this....thank you!
Hi Everyone. Just had my LFT test results today. SGPT (ALT): 9 and SGOT (AST): 15. Still on Viread for the next 6 months. About to start combo with Alinia. Will also quantify HBSAG asap and will post results.
Maybe a separate thread will be a good thing to do.
Also consider to will include all the tests results and treatments in a chronological order and also you will update that thread with new tests like HBsAg and also all test after alinia combo.
Concerning the fatty liver when I had my biopsy in April they found out that I have minimal steatosis. Even though its not much it surprised me anyway cuz I am not a fat person at all and I am doing lots of sports.
Any suggestions what else to do to get rid of all of the fat in my liver?
Dear All. Want to share my latest results with you all.
Viral DNA=2.06 copies per ml (Below quantifiable range)
Liver function: Very Good
SGPT (ALT): 9
SGOT (AST): 22.
Before i started taking Viread (September 2011)
SGPT (ALT): 9 and SGOT (AST): 15.
Still on Viread + Alinia since Nov 2011.
When i was first diagnosed HBSAG + (March 2011)
HBsAG : Positive
Viral DNA=00/ Undetectable
Liver function: Very Good
Hep B Core Antibody: Positive
Anti HBe (igM): Negative
Anti HBe (igG) (H): Positive.
Not still been able to find a place to do HBSAG quantity test in Nigeria. Going to the US next week on a course for 1 week. Really wish I cld locate a place to have it done.
What do u think abt my results so far? Still on Viread + Alinia. Asked my doctor to put me on Peg Interferon. But he said my immune system is working and would clear naturally oveer time.
check posts about indian lab accepting blood samples sent by fedex to test hbsag.
in your case there is no blood test to say anything about your status except hbsag quant (similar to my situation once hbvdna is und only hbsag quant can tell us if drugs are doing any good)
i guess 2 hbsag test at 3 months distance might tell us if it is going down or stable or increasing
Seems like this guy also had same side effect i'm also facing temp , mild fever, muscle ach. 1 week back i took flu medicine also , don't give me hope that my immune system is fighting with virus so quickly and its going to clear ;-)
fever is interferon produced by our body, so when you have fever and muscle ach it is interferon by immune system for hvb or other viruses....it can also be immune system clearing hbvdna with tenofofvir.we will know by 12 weeks when hbvdna should be rechecked
I was on viread for 3years.before starting viread i had no pain.i stopped viread two months ago.i am currently making milk thistle 2000g daily.guess what? The pain has stopped.imagine 3yrs of pain.the itches have been since day one of my infection.after doing my test i willl continue with viread know you can't take viread with milk thirstle
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