Just wondering, I had a liver transplant three years ago. They said the donor had a HBV antibody but they did not detect HBV. I decided to go ahead and go through with the the transplant. The doctors said 1 to 2% chance of HBV appearing. I had been vaccinated (the three shots) about 15 years earlier and so I have HBV antibodies.
After the transplant my doctors said I should go ahead and take Epivir just in case they'd missed something.
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.
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.
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.
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...
who is the crazy docotor who prescribed lamivudine/epivir, add tenofovir as soon as possible, lamivudine don t cure hbv and makes hbv mutations which can be untreatable and can make liver cancer even if hbvdna undetactable
do add tenofovir as soon as possible, you have just worsen your condition with lam, it is not indicated for hbv anymore, only tenofovir (viread) entecavir (baraclude) interferon are
to know if you are clearing you need hbsag quantitative in iu/ml and to know if you are saf
It is 72 hours post-exposure for me right now and I took the triple therapy that I have-- Epivir, Viread, and AZT. I took a dose of Epivir and Viread at 42 hours and then decided I was being paranoid he didn't use a condom [since I only have his word] but read your post and got nervous, so I took a dose of Epivir and Viread late by 6 hours. I started the AZT for the first time at about 72 hours.
All medications come with something called a 'package insert' which has labeling that includes any risks. Did you tell your doctor that you are expecting? I would just call the office to be safe and tell them you are pregnant and want to know if the antibiotic prescribed for you is safe during pregnancy.
This time i decided to check hbv dna. Here was the results today. Alt 6 u/l (6-29 u/l) and ast 14 u/l ( 10-35 u/l) and hbv dna 5500 iu/ml. Throughout my research, i do not believe i need treatment. But they say dna > 2000 iu/ml needs closely monitor, how often? I will talk to my gi doctor soon. Just need some preparation to ask appropriate questions? Any comments will be appreciated. Thanks.
I do have the insert at home. It said if there were NO lines it was inconclusive, but nothing about a line in the circle and nothing in the oval. The way it reads, for it to be positive, there should be a line in each opening. I will be taking another one tonight, hoping it is more conclusive. thanx!
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.
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?
I learned that I had chronic Hep B about 14 years ago. My last DNA test (about 4 months ago) said that the viris was undetectable. I'm still on Epivir.
I have three questions:
1. Being undetectable, should I reveal that I have HEP B to a potential sex partner?
2. If so, at what level of activity should I reveal that I have HEP B-- for kissing, or oral sex, or intercourse?
3. What are the chances of my really passing the viris to someone if I am undetectable?
Thanks for your help.
Temporary headaches, high blood pressure, or a general sense of feeling ill
Nausea
Vomiting
Fatigue
Headaches
Insomnia
Rare cases of hair loss
Tenofovir DF (Viread)
An antiviral drug for people with HIV infection. When taken with other antiviral drugs, it can reduce one's viral load to extremely low levels, and increase one's T-cell counts. Tenofovir may also help control Hepatitis B.
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