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Famciclovir
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O&V Aciclovir and Warts Part 2
To this massive improvement Julian
To this massive improvement Julian
TheFlyer
in
CLL Support
26 days ago
Anyone has a drug reaction to Valtrex and Famir?
Hi, Hope these lines find you well! I am unable to tolerate Valtrex or Famir. Just wondering if anyone has experienced this. I haven't tried acyclovir thinking that it would be same... I appreciate your responses, as I have frequent outbreaks. I'm trying to establish if this a drug reaction or
Hi, Hope these lines find you well! I am unable to tolerate Valtrex or Famir. Just wondering if anyone has experienced this. I haven't tried acyclovir thinking that it would be same... I appreciate your responses, as I have frequent outbreaks. I'm trying to establish if this a drug reaction or
rosegardens
in
BASHH
27 days ago
Prevention Routine?? 5 1/2yrs. on the I/O clinical trial
Hi All, Just wanted to share what I have done to try to stay healthy with reasonable success during my 12 yrs. journey confronting CLL. *Brief History: 84 year old male diagnosed in 2012 with 11q, trisomy 12, unmutated. Normal blood picture except for low platelets, IGG. IGA, and I GM. Currently
Hi All, Just wanted to share what I have done to try to stay healthy with reasonable success during my 12 yrs. journey confronting CLL. *Brief History: 84 year old male diagnosed in 2012 with 11q, trisomy 12, unmutated. Normal blood picture except for low platelets, IGG. IGA, and I GM. Currently
Varney
in
CLL Support
2 months ago
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Doxycycline long term use
Hi, I’m 11 months into my 15 month treatment for CLL. I’m on Ibrutinib with Venetoclax and it’s suited me well, and I’m really pleased that my bloods now appear to be normal. I’m also on Co-Trimoxazole antibiotic and Aciclovir antiviral to deal with any infections should they arise during my treatment
Hi, I’m 11 months into my 15 month treatment for CLL. I’m on Ibrutinib with Venetoclax and it’s suited me well, and I’m really pleased that my bloods now appear to be normal. I’m also on Co-Trimoxazole antibiotic and Aciclovir antiviral to deal with any infections should they arise during my treatment
Smiley60
in
CLL Support
2 months ago
health anxiety and taking medication
hi all, I have health anxiety and overthink and worry about taking any new medication. I have been prescribed aciclovir for shingles and I’m so scared about taking the first one as I’ve seen dizziness is a side affect? Anyone got any advice or taken these before? Thank you
hi all, I have health anxiety and overthink and worry about taking any new medication. I have been prescribed aciclovir for shingles and I’m so scared about taking the first one as I’ve seen dizziness is a side affect? Anyone got any advice or taken these before? Thank you
Kimbad1990
in
Anxiety and Depression Support
3 months ago
Acyclovir for fever blisters?
Some years ago I was prescribed Acyclovir cream for my mouth fever blisters rather than the oral medicine because the oral can raise liver enzymes. However I was recently told that the oral Acyclovir medicine works much faster and the increase in liver enzymes goes back to normal when Acyclovir is stopped
Some years ago I was prescribed Acyclovir cream for my mouth fever blisters rather than the oral medicine because the oral can raise liver enzymes. However I was recently told that the oral Acyclovir medicine works much faster and the increase in liver enzymes goes back to normal when Acyclovir is stopped
Twojer
in
PBCers Organization
3 months ago
New to Rux
Hi everyone. Thank you all for all the useful replies I got to my last question. Two more queries here: I'm newly diagnosed with post-ET Myelofibrosis and I've just collected my first prescription of Jakavi which I haven't taken yet.I noticed that the tablets are 20mg, and I have to take 2 a day. Someone
Hi everyone. Thank you all for all the useful replies I got to my last question. Two more queries here: I'm newly diagnosed with post-ET Myelofibrosis and I've just collected my first prescription of Jakavi which I haven't taken yet.I noticed that the tablets are 20mg, and I have to take 2 a day. Someone
Sivasi
in
MPN Voice
4 months ago
Stem cell transplant (SCT) 15 months on
I'm now 15 months after my SCT and in my my recent review my figures are improving:WBC 4.0 HB 139 Neut 2.3, lymph1.12 and platelets 106 ( highest for a couple of years). I also had my CD4 lymphocytes measured and can now come off Acyclovir and pentamidine. Hooray! I hated those nebulisers. This leaves
I'm now 15 months after my SCT and in my my recent review my figures are improving:WBC 4.0 HB 139 Neut 2.3, lymph1.12 and platelets 106 ( highest for a couple of years). I also had my CD4 lymphocytes measured and can now come off Acyclovir and pentamidine. Hooray! I hated those nebulisers. This leaves
Scaredy_cat
in
MPN Voice
4 months ago
Shingles and Ruxolitinib
I note that on the Blood Cancer web site is states that [i]Aciclovir is an anti-viral medication that prevents shingles, which can be a side effect of Ruxolitinib.[/i] [i]If you’re on Ruxolitinib, you have to be careful about your skin,[/i] I was told to be aware and careful of my skin when taking
I note that on the Blood Cancer web site is states that [i]Aciclovir is an anti-viral medication that prevents shingles, which can be a side effect of Ruxolitinib.[/i] [i]If you’re on Ruxolitinib, you have to be careful about your skin,[/i] I was told to be aware and careful of my skin when taking
nanmc
in
MPN Voice
4 months ago
Shingles & needing more heart surgery
My first mitral valve repair has failed sadly after 3 yrs & I need it redone, more open heart surgery..... but a month ago got Shingles. I was unable to take acyclovir as it made me incredibly dizzy & unbalanced. I am in terrible pain after 4 weeks & no sign of it improving though the rash blisters are
My first mitral valve repair has failed sadly after 3 yrs & I need it redone, more open heart surgery..... but a month ago got Shingles. I was unable to take acyclovir as it made me incredibly dizzy & unbalanced. I am in terrible pain after 4 weeks & no sign of it improving though the rash blisters are
Warm-heart
in
British Heart Foundation
5 months ago
Update on my CLL diagnosis
Hello, I was diagnosed with CLL in Oct 2022 and was told I had # CLL/SLL with extensive bone marrow involvement, trisomy 12, p53 wild-type, IgHV-mutated, Rai stage 3. My oncologist at the Cancer Center put me on the O and V treatment which started in Dec 2022. I finished the O in May 2023 and the
Hello, I was diagnosed with CLL in Oct 2022 and was told I had # CLL/SLL with extensive bone marrow involvement, trisomy 12, p53 wild-type, IgHV-mutated, Rai stage 3. My oncologist at the Cancer Center put me on the O and V treatment which started in Dec 2022. I finished the O in May 2023 and the
tenniselbowz
in
CLL Support
5 months ago
Still uMRD 1 year later after fixed duration A&O combo
Happy to share that after finishing treatment 12 months ago, my new Clonoseq results still show zero residual clonal cells from a 3.4 million sample! Glad to be off medication of any kind for a year. (with the exception of Acyclovir.) It’s a great feeling.
Happy to share that after finishing treatment 12 months ago, my new Clonoseq results still show zero residual clonal cells from a 3.4 million sample! Glad to be off medication of any kind for a year. (with the exception of Acyclovir.) It’s a great feeling.
Kvb-texas
in
CLL Support
6 months ago
HSV 1
Hello. I need some advice. My brother was diagnosed with HSV 1 Encephalitis on January 12. And on January 9 he had an epi attack. He was in the hospital for a month, he was treated with acyclovir. The last lumbar puncture was negative for the virus. He has been receiving home treatment since February
Hello. I need some advice. My brother was diagnosed with HSV 1 Encephalitis on January 12. And on January 9 he had an epi attack. He was in the hospital for a month, he was treated with acyclovir. The last lumbar puncture was negative for the virus. He has been receiving home treatment since February
Recnik
in
Encephalitis International
6 months ago
Suspected Vulvadynia? Severe and constant clitoris pain/burning with some pain underneath. All exacerbated by sitting/walking/weeing.
Me and my husband had sex over 6 weeks ago a few days after I began with burning type pain mainly at the front around my clitoris but it did seem to radiate underneath. I began drinking lots of water thinking I have cystitis. 1 week later I saw a GP and although my urine sample was negative to any
Me and my husband had sex over 6 weeks ago a few days after I began with burning type pain mainly at the front around my clitoris but it did seem to radiate underneath. I began drinking lots of water thinking I have cystitis. 1 week later I saw a GP and although my urine sample was negative to any
Redskytonight
in
Pelvic Pain Support Network
6 months ago
Remission but suddenly extreme night sweats
I received the good news that I am in complete remission......no cancer cells in my blood.... but unfortunately I was just diagnosed with Gastritis due to the Venetoclax and Aciclovir. It's very painful but after stopping all my cancer medication the stomach pains and diarrhoea are easing off. But
I received the good news that I am in complete remission......no cancer cells in my blood.... but unfortunately I was just diagnosed with Gastritis due to the Venetoclax and Aciclovir. It's very painful but after stopping all my cancer medication the stomach pains and diarrhoea are easing off. But
MalcT
in
CLL Support
6 months ago
Solutions needed to manage nerve pains ( Post herpetic neuralgia ) after shingles .
I was diagnosed of CLL in 2021. Had FCR as first line treatment. Was on remission for about a year before relapse. Currently on Ibrutinib since 5 months now. I had shingles on my left leg about 3 months ago. Was treated with Acyclovir. The sores and blisters have gone but the nerve pains( especially
I was diagnosed of CLL in 2021. Had FCR as first line treatment. Was on remission for about a year before relapse. Currently on Ibrutinib since 5 months now. I had shingles on my left leg about 3 months ago. Was treated with Acyclovir. The sores and blisters have gone but the nerve pains( especially
Oldscores1
in
CLL Support
7 months ago
Aciclovir as prevention for shingles
I wish to express my deepest thanks to all fellow members who have responded to my recent enquiry. There has been consensus in all replies confirming that prescribing Aciclovir is standard practice.
I wish to express my deepest thanks to all fellow members who have responded to my recent enquiry. There has been consensus in all replies confirming that prescribing Aciclovir is standard practice.
RamsesII
in
CLL Support
7 months ago
Herpes (or acyclovir usage) affecting implantation after ivf embryo transfer?
I have had herpes for about 10 years. I have noticed more outbreaks during stims. I've already had 2 failed transfers and am worried both that having herpes and /or taking acyclovir will affect implantation for my last transfer. I've read some conflicting studies on acyclovir and it's effect on implantation
I have had herpes for about 10 years. I have noticed more outbreaks during stims. I've already had 2 failed transfers and am worried both that having herpes and /or taking acyclovir will affect implantation for my last transfer. I've read some conflicting studies on acyclovir and it's effect on implantation
Norregirl
in
Fertility Network UK
7 months ago
Replacing Acyclovir.
I’m trying to keep my one kidney from all medications that cause harm. Does anyone know of an antiviral that I should use instead of acyclovir? Thank you.
I’m trying to keep my one kidney from all medications that cause harm. Does anyone know of an antiviral that I should use instead of acyclovir? Thank you.
Fredismydog
in
Non Hodgkin's Lymphoma Friends
7 months ago
a safe antiviral.
Being that I was born with Solitary kidney and started on acyclovir when I started chemo, I’m trying to find an antiviral that doesn’t harm my kidney. Has anyone got some leads for me? Thank you.
Being that I was born with Solitary kidney and started on acyclovir when I started chemo, I’m trying to find an antiviral that doesn’t harm my kidney. Has anyone got some leads for me? Thank you.
Fredismydog
in
Kidney Disease
7 months ago
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