Epivir=Lamivudine, said to be very safe for husband and wife who wish to have children. But do you have to choose Lamivudine as first-line treatment with its high resistance profile?
t remember, should I take the AZT with my Viread and Epivir for a more potent PEP regimen? Or is Viread and Epivir alone okay? I have no side effects from them.
Given that this is a gay sex club in NYC, an epicenter of the epidemic? Is it possible to forget having anal sex as a top? I am not a frequent visitor to sex clubs. I do have a phobia of "forgetting" anal sex when I'm drunk- though I've never forgotten it ever before.
I treated with hep b 14 years ago for 1.5 years with epivir and got hbv e antibodies and afterwards, I stop epivir and every 6 months I check my liver function and alt and ast are persistently normal. I started to check hbv dna 6 months ago as new guidelines come out. Hbv dna at six month was 5000 iu/ml and last week I checked it was 8000 iu/ml. Again both times my alt and ast are normal. As a matter of fact they are in low side of normal.
Hi everyone,
I went to see my Dr today and he recommanded to change my medicine to Viread (I am on Epivir more than 2 years). I am wondering if it's necessary to change it now since Epivir works well with me (my DNA is 200 copies). But he was worried about resistance and mutation. Do I have to listen to him? I got Viread today but I am not sure I would start taking it from today.
-Natalie
p.s.: Do you guys drink coffee? I started drinking coffee about 4 months ago...
I was diagnosed Hep B 13 years ago, and have taken Epivir since 2002. I do blood test and ultra-sound every 6 months and Hep B is controlled pretty well. As you know, Epivir cause virus mutant resistance, and chance is higher for me since I have been on it for 5 years. My doctor gave me 2 choices,
1) "don't fix it until it breaks" - continue with Epivir, move to combo treatment when mutant and resistance evidence shows up.
2) "precautious way" - take baraclude.
The drug can cause side effects such as flu-like symptoms, depression, and headaches. Approved 1991 and available for both children and adults.
Pegylated Interferon (Pegasys) is given by injection once a week usually for six months to a year. The drug can cause side effects such as flu-like symptoms and depression. Approved May 2005 and available only for adults.
1 Does this mean I do not respond to Tyzeka?
2. Should I change to Ziread since it is approved.
3. I have experienced elbow pain, left arm, with Tzyeka.
4. Does changing drugs instead of stopping altogether cause flare up?
Previouusely I took EPIVIR for 7 years and Hepsera for one year.
Thank you.
Antivirals such as Entecavir (Baraclude), Telbivudine (Tyzeka), Tenofovir, Adefovir (Hepsera), lamivudine (Epivir-HBV) have less upfront side effects but their long term consequences hurt patients even more: possible lifetime dependency, resistence issue, cost burden, toxicity, possible link to neuropathy, nephropathy and cancer, etc. With all these consequences the cure rate is a miserable below 1%! That is why I choose to manage my chronic HBV with foods, herbs and adjusted life style.
I was wondering given the following conditions - 1) HBV is UND (<357/IU) 2) On Epivir for the last several years because after some surgery the doctors thought it was possible I had been exposed to HBV or got some tainted blood 3) previously had the HBV vaccine 15 years ago. 4) No signs of HBV.
However, I was prescribed Combivir and Epivir (only-not a third drug) for 28 days and during this time I had a cold with a sore throat and headache for almost the whole period up to a few days ago. It is now almost 7 weeks since I had the sexual encounter in Bangkok. After 30 days I had an HIV test and the result was negative. I am now going to have a test at 8 weeks. I am worried to death and I wonder if the PEP I was prescribed has been wrong or not sufficient.
I will do that it seems the higher dose has created this and I'm not on anything else.
Many AD's have side effects that affect the libido, guess it applies to both sex es. As far as I know all AD's have this drastic effect . Hopefully you'll find one that's OK for you . Good luck.
Yes, I've only been on it a week and I experience the muscle aches and bilateral flank pain as well. In addition, insomnia!
THOUGHT I WAS GOING CRAZY BEFORE I FOUND YOU GUY. SIDE EFFECTS MUCH MORE THAN WE HAD BEEN LED TO BELIEVE.PERSONALLY HAVE THE BLURRY VISION, ENHANCED JOINT PAIN, SWEATS, AND SLEEP NOT GOOD. FINALLY SAW FEED BACK FROM THE COMMUNITY THAT VERIFIED OTHERS FEELING SAME. ANYONE FEELING ANYTHING ELSE ODD? PLEASE POST. ALSO HAVE BLOATING, IRRITABILITY. AND CONTRARY TO WHAT DOCTORS SAY, I'M ALWAYS CONSTIPATED.
Hi. I am on week 60/72, second round of treatment. I was really really sick after shot for first few months and then this resolved and became tolerable at least. I now find that I am having these same significant side effects later in tx. This didn't happen last round, but I went 48 then. Anyone else have this happen?
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