I was also a reciever. After 40 hours I went to the first clinic and they gave me PEP (TenofovirDF, emtricitabine + lamivudine). The clinic looks very unprofessional, but it was my only chance. I didn't do any hiv or std test, a month before the exposure i had HIV test which was negative. After few days I had a mild sore throat, i still have it, i don't have fever, running nose, rash or anything else. My questions are..
An international study found the antiviral combination of tenofovir and emtricitabine (Truvada) was most effective in treating younger adult hepatitis B patients with high viral load and normal ALT levels.
Doctors historically have not treated this group because there appeared to be no sign of liver damage. However, doctors now know that high viral loads may increase patients’ risk of liver damage and cancer as they age, despite their normal ALT levels.
What are my chances of getting infected. Another question was administered a PEP drug emtricitabine and tenofovir, can it prevent me from contracting HiV.
FTC is Emtricitabine.
This is a potential concern because the drugs in Truvada – tenofovir and emtricitabine – are active against HBV as well as HIV.
HIV and HBV are spread through some common transmission routes, including sexual transmission, vertical transmission (mother to child) and via multi-person use of injection equipment.
I asked her of her status and she stated clean. I started PEP within 24 hours. (Teneogovir, emtricitabine, lamivudine ) What are the odds of being infected ? is this low risk ?
I started a course of PEP that included Tenvor-EM (Indian version Emtricitabine/Tenofovir DF) and Kaluvia (generic of lopinavir/retonavir) for 25 days and interrupted it for two reasons:
1-My partner tested Negative(Antigen/ Antibody) on 22 days post exposure
2-Thinking that i might be developing facial Lipodystrophy (slight facial fat loss under cheek bones). I cant tell if my face was like this before the treatment or it is just an illusion.
Good afternoon. There is a double-acting drugs - lamivudine, emtricitabine, tenofovir. This is known. Are there any similar action in the protease inhibitor, such as Kaletra (lopinavir) for example?
Have you ever thought about that?
I read - sometimes laugh. Simvastatin, vitamin D, which the Chinese poeben, mythical new drugs, masturbation with measurements of the level of HBsAg, and other nonsense....
m thinking about taking Tenofovir only because I will move to a place where Emtricitabine is not available. I know it is better to combo. But can you tell me how risky it is if I take tenofovir only (LAM resistance)? stef2011?
truvada is just tenofovir+ftc, it is sueless on hbv unless non response to tenofovir, which is extremely rare
it adds toxicity and higher price because truvada patent is not expiring in 2014, no difference on hbsag.
instead of truvada it is best only for those non responding to combo tenofovir+lamivudine.
the second component is unchanged, 200mg of emtricitabine, also called FTC, a fluor substituted form of Lamivudine, that provides protection from the development of mutants that will lower the responsiveness to tenofovir.
it's side effects are generally considered very mild, equivalent to lamivudine.
This is theoretically good news for hbv patients waiting eagerly for TAF to be available for HBV.
The problem is the high price: 1500$ for one month supply of 30 pills.
You are correct that Truvada is a combination of tenofovir and emtricitabine, and is generally prescribed for patients with HIV. Being a HBV forum, most of us know very little about Truvada except that it is prescribed off-label for HBV by some doctors, and that it is recommended for HBV patients who develop resistance to Tenofovir.
I have burning in the bottoms of my feet, as well as neuropathy in feet and hands. The neuropathy is caused by years of untreated pernicious anemia, so if you haven't been tested for B12 deficiency, you should ask your doctor to do so. I'm not sure about the burning in the bottoms of my feet. I don't think it's thyroid related, but at this point, I can't say.
I am 2 chemos away from finishing my round of six and have developed peripheral neuropathy in my hands and feet. I am on 300mg Neurontin 3 x a day and it still seems to be getting worse. The pain keeps me from walking long distances and I cannot hang my hands down; I have to keep my elbows bent. I have also tried acupuncture. I use warmth to alleviate the pain but it is only a temporary relief. Any ideas or experiences?
hi hubby on wk 14 of triple tx they say it will stop his perpheral neuropathy getting any worse which is why he agreed to have the hep c treatment in first place because he got no other symptoms normally associated with hep c his scan and liver function tests are more then alright for a 61 yr old and has you good folks out there you know this treatment is very hard for all concerned any info will be greatly appreciated many thanks
Hi,
Benign neuropathy is usually the treatable form of neuropathy. It occurs mainly due to diabetes or B12 deficiency. It can be controlled by maintaining the sugar levels in the normal range and by B12 supplementation.
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