I 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 RepliesAfter 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 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 have been on flu 40 mg for 12 weeks now and it seems that in the last week I have been feeling worse again.
It's a strange feeling but I feel indifferent to myself and seem to not care at the moment about my actions and thinking that what I do is not a problem?
I was just wondering is it possible with depression to still have days when you feel down and want to give up?
I'm just wondering how many weeks all the smokers were when you stopped smoking?
View 14 RepliesStarted 24 week treatment with Harvoni 1/20/15 Genotype 1-a Stage 4 Cirrhosis with Compensated liver
Ast 123 then, 45 now
Alt 165 then, 165 now
Viral load then: 2,600,000 now less than 15
Hep C still detected but I thought this was great for the 1st 4 week prognosis since I am on pill for 24 weeks.
How is everyone else doing?
Just completed 12 weeks sovaldi , Peg and CoPeg ......awaiting blood work results to see if I cleared the Hep C 3 Virus . While I tolerated these drugs fairly well , I am concerned that in the 12 weeks of treatment the liver enzymes which are 150 to 200 respectively , never went back to normal. It seems that my situation may be an anomaly.
View 1 RepliesTreated for HCV Genotype-2 with Sovaldi & Ribavirin for 12 weeks.
Came up undetected half way and drawn full labs today to be read 6/6/14 to me on my follow up.
The proof in the pudding will be for Labs drawn in 1/15.
My sides were mostly nausea but frequent water and making my meals smaller and more frequent all but eliminated that. Three regular meals a day seemed to leave my stomach unprotected in-between. So smaller and more often did the trick.
The Sovaldi seemed to make me hyper. I noticed an hour or so after taking it I seemed to have lots of energy.
Periods of general yuck feeling would come and go, and in different strengths.
Sometimes keeping busy helped and sometimes nothing but the couch would give me comfort.
I took the Riba in the AM, the Sovaldi mid day and the Riba again in the PM.
Its been a long row to hoe over 9 years. Two stints of Riba & Interferons, 12 and 48 week terms both relapsing, then on the interferons only @ half dose to maintain while waiting for something new.
Then as a result of all this diabetes and neuropathy set in causing the maintaining regimen to be discontinued.
I don't drink or smoke, I did it all as correctly as possible.
I am genotype 1, had liver transplant in 2001, treated and relapsed after 72 weeks of Interferon and Riba in 2006/7. Possible cirrhosis, as biopsy shows F1 and but Fibroscan shows 27 kPa. Have controlled HE (Xifaxan) and some ascites on CT scan. PCR at four weeks showed presence of virus at less than 43 (13 million in January).
Amazed at the improvements compared to the day I started treatment.
Start/after four weeks of tx
ALT: 59/31
SGOT: 61/36
Albumin: 3.1/3.7
Bilirubin: 1.6/1.6
Platelets: 126k/132k
HGB: 11.9/12.4
ALP: 273/196
GGT: 1283/543
INR: 1.0/1.1
Ammonia: 52/35
Creatinine: .8/.8
The values for Alt, Sgot, Albumin, GGT, and alk-phos are the best I have had in three years. Can’t wait so see how they look at end of 24 weeks.
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 RepliesHas anyone used testosterone gel to help with the bedroom but i've just been prescribed by my gp.
View 12 Replies