After 1month of viread, my alt increased from 200 to 373.
Before:
Hbv DNA 170 million
As I said my Sgpt 200
Hbeag reactive
After 1 month
Hbv DNA 133,000
Hbeag reactive
Sgpt 373
My alt increasing is this normal?after 2 more months what will be next happen to my sgpt.please share with ur tdf experienced.
I have been diagnosed with Hep B. I was admitted to hospital with exceptional readings (ALT >4,000, bilirubin 180, all pho 162, gamma get 417, AST >2,500). I've been given various drips and the numbers are coming down. ALT has now halved. In addition to the drips I was also put on Viread.
My physician was concerned how my immune system was attacking the liver and between all treatments, in three days the readings are coming down. My jaundice is going and my urine now looking paler (almost normal).
Given the symptoms indicate a severe acute response to infection, does this suggest my body will put up a good fight to rid itself of the virus. Also, is there a risk Viread could actually lead to my body not developing the antibodies? I've read the following study, which suggests Viread can be highly effective in treating severe acute Hep B and also assist (or at least not inhibit) the development of antibodies.
I ve been on viread for 3 months. The latest hbv dna is positive <20 ıu/ml. Before viread I was on lamivudine and hbv dna was generally again positive <20 ıu/ml. I think it was 3 times undetectable at different times. Alt Ast normal afp normal. Do you think dna will be und next time? If it comes positive again what. treatment or evaluation can you recommend ? I also started to take vit d3 daily 10 days ago.
View 6 RepliesI have hepatitis b infection in the liver. I need your advise if I should take viread medication if I have osteopenia and my kidney is not the best? I am currently taking osteopenia pill. Please advise and help. Thanks a lot. I am worried about viread side effects on me. Another question is if I take the medicine, can I ever stop taking the medicine? Is it a life term medicine I have to take?
View 1 RepliesI want to know..if continue taking this..viread.my liver is going to serious damage?.my lab result before taking viread.
Hbv DNA - 170 million
Sgpt - 200
Hbeag - reactive
After 1 one month of taking tdf.
Hbv DNA - 100,000 something..
Hbeag - reactive
Sgpt - 337
My Doctor prescribed a viread/ tenofavir.shall i take it.Is it a safe antiviral drug.What can i expect as a side effects?
View 2 RepliesMy doctor let me have Viread. I checked online at pharmacy checker. Tenofovir Disoproxil Fumarate Tablet and Viread Tablet, are they the same in treatment wise? I went to CVS store, it cost 1000 USD to 30/300mg for Viread Tablet. is it too expensive? The staff there told me generic tablet is not available. But why I see it online as I said earlier?
What happens if I take brand and then switch to generic like a year later? Will the generic medicine do the same?
So I've been taking viread before bed for the last 4 years. My hair has been receding and falling out throughout those years. It is now getting really aggressive and noticeable. I stopped taking viread for a month to see if it would reverse and sure enough it did. It came back full and thick. Yesterday I took viread again and half of what came back began falling out. Does anyone have any tips or suggestions? I'm still young and my parents have good hair. What can I do to stop or prevent? I tried taking biotin but it seems its not enough
View 16 RepliesHas anyone experience nail discoloration after starting viread?
View 11 RepliesI just had my second child 7 weeks ago. I stopped taking VIREAD FOR 3 weeks after gave birth because of breastfeeding. But ALT was increased to 53. Then I continue to take VIREAD but now the ALT is still 53. I remember this medicine can control liver function very quick when I started to take it years ago. is it possible the medicine doesn't work on me anymore? anybody can explain?
View 1 RepliesWhen I first began treatment with pegasys in january 2014, GGT was 60 (normal max is 35), ASAT 51 (normal max 35), ALAT 76 (normal 10-40), LDH/Bili/CK all within normal range. With pegasys, a few months later down the line, the values continued to go higher. At their highest, GGT 223, ASAT 116, ALAT 156, LDH 274, Bili/CK remained within normal range.
At the beginning of the treatment, Hep B ie/ml was 2400. Four months later, it became 2600. When I was shifted to tenofovir/Viread three or months after beginning treatment since pegasys wasn't solving the issue, the ASAT, ALAT, LDH came back down to normal levels quite fast. So I have been on viread ever since.
10 months after beginning treatment, Hep B ie/ml was down to 1800. In 2015, it was less than 150. Hep B Dna was undetected by May 2015. I get regular blood tests every three months since the start of the treatment.
Yesterday's blood test showed: ASAT 36 (normal max 35), ALAT 38 (normal 40, but having checked past blood tests, it seems in the last few months it has been gaining one or two points steadily so this is worrying me), LDH and Bili are normal. The bad news: Heb B DNA detected...and IE/ml was a whopping 3400!!!! More than when I started started treatment!
The first thing I was asked was whether I missed a dose of viread. Answer is no. However, I have had incidents where I did forget to take it on time, but it has never exceeded 5 hours (still, I know, it's a huge gap). Not a lot of times, but I find that I am beating myself over this now, as it may be the reason I am having a viral overload and maybe made the virus resistant to viread.
Since taking viread, I have experienced and continue to experience extreme muscle pain (I ended up in the hospital once when diclofenac failed me and I needed an extra morphine shot to get relief). I am continuously tired, some days it is a real struggle to move (feels like going through mud - heavy body, wanting to simply just crash on the floor). I have not had a pain free day in the last two years and worse, kidney stones! I am already prone to them, but I can't get over the suspicion that Viread has ensured I have a stone that needs to be taken out each year.
I've read that viread is one of the best treatment there is (hardly any side effects, probability of virus resistance low) so my latest blood test is worrying me no end. I am not due for another DNA test until 6 months later. I've also read that ASAT and ALAT values can increase and it's not necessarily liver related (I think my ongoing and increasing muscle pain is reflecting higher ASAT and ALAT values but who knows?!?).
My doctor says that as long as those values remain within normal range and not in the hundreds, it should be ok. But there is this unspoken thought that I am in deep trouble if the DNA continues to manifest and my liver enzyme values continue to increase. My liver scan in 2014 has me a point JUST before entering cirrhosis stage. I can't help but think I may have actually crossed that line already (the cassandra in me speaking) though I am assured that viread treatment tends to pull back the damage.
My question..Has anyone ever experienced a viral increase during the viread treatment, and if so, was it temporary, or was viread stopped? I am not sure how to read/interpret this ie/ml, but the fact that it has increased can't be good news at all.
I have been on Viread for three years and my viral load never goes undetectable. The viral load went down in the past two years. However, it has been up and down in the range of 100 to 300 IU in the past year. It seems that it will never go down to undetectable. The test for mutation failed three times because of very low viral load. Am I non-responder to Viread? Should I switch to another treatment? Should I be concerned?
View 13 RepliesThere is a link about tenofovir alafenamide (TAF).
View 7 RepliesI'd like to relate our experience with Hep C treatment. My husband got Hep C back before it even had a letter, in the 1970s, and he is now 62. He has never been much of a drinker, which is very fortunate. He has always had a ridiculous amount of energy, and an active occupation. He kept an eye on his liver (don't take that literally!), and the diagnosis never much affected him. But after a divorce about 10 years ago, he began to consume more alcohol than before, and his liver enzymes crept up, and his biopsy in 2009 said he had Stage 4 cirrhosis. Yet function was still fine, and still he did not feel affected by the disease. The doc said, the numbers say it's time for interferon.
The side effects and prognosis for cure were not encouraging, and I contacted naturopaths I know to get a recommendation for someone for him to see. They recommended a doctor at John Bastyr Naturopathic College in WA State, and we went to see her. She specializes in traditional Chinese medicine for cancer, HIV and liver diseases. She prescribed an herbal combination, and some other supplements. And ZERO alcohol. She was the first doctor who actually said NONE. Other doctors would pussyfoot around and say, don't drink a lot, but no one said, don't have any at all. Not even one beer on Friday. Not drinking was not a problem for him, as he had already mostly stopped having any once he got the Stage 4 pronouncement.
The treatment regimen she started him on made him feel worse, so he went back, and she put him on a different formula, something called Livercel, made by Nutricology. It contains a proprietary blend of Patrinia extract, Phellodendron amurense extract, Yi-Chen wormwood extract and Schisandra extract. He also was taking milk thistle and a few other things. This herbal combo reversed the numbers, brought his liver function (alt and ast) down to high normal, whereas they had been going way up.
He kept to this regimen and was going along fine, back to not feeling impacted by the virus, though of course he knew it was still there. However, at his checkup last June, his numbers were starting to go up again, and now that there was a real cure available, his naturopath said, ok, now the new drugs have been proven effective and have minimal side effects, so time to give that a try, if you can afford it. Which of course, hardly anybody can. So then we started on that journey.
Meanwhile, what my husband hadn't mentioned to me was that because he was feeling so unaffected by the disease, he had started being not so diligent about taking the Livercel. Taking it once a day instead of twice, or skipping a day, etc. Once he got the higher numbers in June, he started taking them religiously, never skipping. And you know what? HIS NUMBERS WENT DOWN AGAIN. The RNA quantitation was 15,774,971 in June, and on the 11th January, it had gone down to 6,646,637. Down about 60%. This shows to me that the Livercel was having effect. So look into that while you are waiting for the new medicines to be available at a reasonable price.
Meanwhile, although his allopathic doctor's request for Harvoni was initially denied by the health care insurance company, they approved it when she resubmitted it. And they signed him up for the Harvoni's patient co-pay subsidy. He has been on it for a week, and so far no side effects at all. I asked him if he felt anything at all yet, and he said, "I think they must have given me the placebo.
my father is 66 years old, it has been found out through blood test (ANTI HCV) his cutoff value is 1.00 and patient value is 12.51. which further reveals reactive hepatitis. what do you suggest for him?
View 1 RepliesI have been suffering from some internal Hemorrhoids that prolapse after a bowel movement for almost a decade. After they prolapse i gently insert them back into where they belong and it has been ok and hasn't affected my life much.
However the past a few days ago after making a bowl movement i noticed when they prolapsed they were very inflamed and large and painful, i couldn't put them back inside me. I waited until the next morning but unfortunately the couldn't go in so i had to go to a hospital. The doctors managed to insert them back in when they applied some gel but it was painful and not easy.
Then 2 days after same problem but they kept on bleeding, had to go back to the Hospital and same thing.
I hope they get better more manageable soon but i doubt it.
Anyway i really want to avoid the traditional Hemorrhoid surgery as i have read the horror stories on here about being in pain for 4-8 weeks, complications and also i can't afford to take so much time off work.
Hence why i am considering the HAL/RAR Procedure, from my research it is less painful and hypothetically you can be off work for only 48 hours.
has anyone experienced this procedure? What was the pain like?
I'm scheduled for a c section Wed. due to my little man's position and the doctor said a vaginal birth could be risky due to the size of my birth canal. I'm a ftm and this really dissapointed me. I'm really scared considering i've never had any surgeries before lol. Has anyone else had a c section? what was your experience? what should i expect?
View 13 RepliesI am told that I need TURP for my enlarged prostate problem . could anyone recommend a good Urologist in Dallas Metroplex area who has good experience in this procedure
View 64 RepliesOver the last 12 months I've had nine or ten endoscopies. The first few were emergencies and I was not very aware of what was happening due to being fully knocked out.
Having survived the initial trauma, I now attend every 1 to 2 months for regular endoscopy checks. I had decided to try without sedation (just the spray) but the consultant virtually insisted that I have sedation. I was a bit annoyed at first at not being given much choice in the matter. They now use the spray and 3 mg of Midazolam each time. In ten seconds, I'm completely out of it and only wake up in recovery. No significant after effects and I'm usually off home in about an hour. Sometimes it goes really easily for the consultant and other times he experiences difficulties with me. Fortunately, the only time I know anything about these difficulties is after the procedure in recovery room.
I see many posts regarding experiences with HOLEP surgery but they all seem to be at least a year old. I am hoping to see some recent posts.
View 1 Repliesi am really struggling with my fibro. The doc has told me to persevere with this tablet. He has also gave me an anti sickness tablet. I would like to know people's experiences with this please.
View 12 Replies