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cytoxan
has anyone declined cytoxan and had success with cellcept in treating kidney injury? My son has had Eculizumab and Rituximab with no success and is now declining rapidly with kidney function.
has anyone declined cytoxan and had success with cellcept in treating kidney injury? My son has had Eculizumab and Rituximab with no success and is now declining rapidly with kidney function.
Vegitarianmom
in
Parents of Children with Kidney Disease
5 months ago
three weeks of ear infection now at breaking point
Here’s what they gave me: [i]
Ciloxan
drops, Flucloxacillian 500mg and Otomise spray but I won’t use that I’m positive that’s how I got T in the first place. [/i] I’m not sure what I’m asking for or if I’m just ranting lol
Here’s what they gave me: [i]
Ciloxan
drops, Flucloxacillian 500mg and Otomise spray but I won’t use that I’m positive that’s how I got T in the first place. [/i] I’m not sure what I’m asking for or if I’m just ranting lol
djv1985
in
Tinnitus UK
1 year ago
chemo
I was diagnosed last fall with limited GPA (in my ears). Was on methotrexate and low dose prednisone until a few weeks ago. Diagnosed with breast cancer in may so taken off the methotrexate when I started chemo last week. One of my chemo drugs is cytoxan. My question is, has anyone else had this
I was diagnosed last fall with limited GPA (in my ears). Was on methotrexate and low dose prednisone until a few weeks ago. Diagnosed with breast cancer in may so taken off the methotrexate when I started chemo last week. One of my chemo drugs is cytoxan. My question is, has anyone else had this
BellaSarge
in
Vasculitis UK
1 year ago
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Struggling to understand all this.
Been dealing with KD for 1.5 years. My doctor has me on a variety of meds that includes-BP, Chol, Lasix,Farxiga,Eliquis, Cytoxan and Prednisone-plus a few more. Always tired. My current EGFR-49, my creatinine level is-1.47, and my urine/protein-14.34. I am suppose to start Rituximab Infusion as
Been dealing with KD for 1.5 years. My doctor has me on a variety of meds that includes-BP, Chol, Lasix,Farxiga,Eliquis, Cytoxan and Prednisone-plus a few more. Always tired. My current EGFR-49, my creatinine level is-1.47, and my urine/protein-14.34. I am suppose to start Rituximab Infusion as
Hidden
in
Kidney Disease
2 years ago
Oral Cytoxan in conjunction w Avastin infusion
I just wanted to report in. My CA 125 has been kept nicely low via Avastin infusions every six weeks. Over the last few months I noticed a trend of it slowly creeping up, Ie, a two point increase each time. I knew that this was odd and my oncologist agreed. I have started 50 mg oral cytotoxin once a
I just wanted to report in. My CA 125 has been kept nicely low via Avastin infusions every six weeks. Over the last few months I noticed a trend of it slowly creeping up, Ie, a two point increase each time. I knew that this was odd and my oncologist agreed. I have started 50 mg oral cytotoxin once a
Leniko
in
My Ovacome
2 years ago
medication question-Cytoxan (oral)
Has anyone been on oral Cytoxan 50 mg daily to stop tumor growth? If so, what has your experience been? Thank you.
Has anyone been on oral Cytoxan 50 mg daily to stop tumor growth? If so, what has your experience been? Thank you.
Leniko
in
My Ovacome
2 years ago
What next after Ibrance? - Verzenio, Kisquali, Xeloda & more
Dear friends, After 1.5 years on Ibrance/Fulvestrant and a very short time in NED status (great while it lasted...) my cancer reappeared this spring. I've just had an axillary lymph node dissection, removing all the known cancerous spots, and now the question is what will be my meds going forward.
Dear friends, After 1.5 years on Ibrance/Fulvestrant and a very short time in NED status (great while it lasted...) my cancer reappeared this spring. I've just had an axillary lymph node dissection, removing all the known cancerous spots, and now the question is what will be my meds going forward.
LDR1
in
SHARE Metastatic Breast Cancer
2 years ago
What's next?
Hi all you wonderful women/lovely ladies. Have any of you ever had a chemo called Topotican (sp?) or Gemzar? The Avastin and cytoxan doesn't seem to be working. I go for another cat scan next week to see what's going on. My CA 125 keeps rising and I'm starting to feel bloated and achy. I don't know what's
Hi all you wonderful women/lovely ladies. Have any of you ever had a chemo called Topotican (sp?) or Gemzar? The Avastin and cytoxan doesn't seem to be working. I go for another cat scan next week to see what's going on. My CA 125 keeps rising and I'm starting to feel bloated and achy. I don't know what's
Cher96
in
My Ovacome
3 years ago
Cytoxan(Cyclophosphamide
Hello to All, My husband had an appointment with his neurologist today. The latest MRI indicates he still has Encephalitis. With the latest cocktail of meds, (prednisone, mycophenolate and Rituxan) his doctor thought the encephalitis would show improvement or be totally gone by now. His doctor
Hello to All, My husband had an appointment with his neurologist today. The latest MRI indicates he still has Encephalitis. With the latest cocktail of meds, (prednisone, mycophenolate and Rituxan) his doctor thought the encephalitis would show improvement or be totally gone by now. His doctor
NebraskaTexas
in
Encephalitis International
3 years ago
Anyone have any experience and personal opinions on the drug Cytoxan. This is a last ditch treatment for me :-(
😊 thank you
😊 thank you
Ashkaren
in
My Ovacome
3 years ago
In need of advise for my father
Hello everyone. My father was diagnosed with metastatic stage 4 PCa in another country (2017). He immediately had bi-lateral orchiectomy, and thereafter when the PSA began to rise, he was prescribed Xtandi (lasted ~6 months) and subsequently had some radiotherapy to the pelvis and spine (pain management
Hello everyone. My father was diagnosed with metastatic stage 4 PCa in another country (2017). He immediately had bi-lateral orchiectomy, and thereafter when the PSA began to rise, he was prescribed Xtandi (lasted ~6 months) and subsequently had some radiotherapy to the pelvis and spine (pain management
AerospaceElectrical
in
Advanced Prostate Cancer
4 years ago
Anyone doing Euro Lupus protocol? (Low dose cyclophosphamide)
Hello to everyone out there! I’m new to the group - seeking advice from those who have undergone the Euro Lupus Protocol? This is cytoxan (cyclophosphamide) treatments by IV every other week. I understand infusion treatment takes approximately 6 hrs. Sounds very looong to me! What does one do all
Hello to everyone out there! I’m new to the group - seeking advice from those who have undergone the Euro Lupus Protocol? This is cytoxan (cyclophosphamide) treatments by IV every other week. I understand infusion treatment takes approximately 6 hrs. Sounds very looong to me! What does one do all
Tired-in-Toronto
in
LUPUS UK
5 years ago
ASCO 2019 Abstract Recap
The annual American Society of Clinical Oncology (ASCO) conference encompasses multiple types of cancer, and this year many abstracts were submitted about MBC. I’ve reviewed the abstracts and taken the liberty of pasting information about those that were not previously in my book, “The Insider’s Guide
The annual American Society of Clinical Oncology (ASCO) conference encompasses multiple types of cancer, and this year many abstracts were submitted about MBC. I’ve reviewed the abstracts and taken the liberty of pasting information about those that were not previously in my book, “The Insider’s Guide
Bestbird
in
SHARE Metastatic Breast Cancer
5 years ago
Day 2 of hospital
Well I had an appetite today for the first time in 12 days! Food sucks but edible. I think I ate too much even though I still didn’t eat much... For some reason they didn’t start my chemo until super late last night so now it won’t be done until late Friday night. I was very lucky to have visitors
Well I had an appetite today for the first time in 12 days! Food sucks but edible. I think I ate too much even though I still didn’t eat much... For some reason they didn’t start my chemo until super late last night so now it won’t be done until late Friday night. I was very lucky to have visitors
rlyndecker
in
CLL Support
6 years ago
Just diagnosed - vasculitis GPA
Hi, I am so glad I've found this site as I am just at the start of my vasculitis journey and from what I read, seen and heard I will need all the help I can get. I suspect my immune system got triggered when I donated blood in August 2018 - I got really sick during the process. Nothing unusual, it happens
Hi, I am so glad I've found this site as I am just at the start of my vasculitis journey and from what I read, seen and heard I will need all the help I can get. I suspect my immune system got triggered when I donated blood in August 2018 - I got really sick during the process. Nothing unusual, it happens
NacMacFeegle
in
Vasculitis UK
6 years ago
My journey
Hello I was diagnosed in 2006 with BC in the right breast stage 11, lymph node involvement 4. Treatment lumpectomy, 6 cycles every 3 weeks of a cocktail of Taxotere and Adriamycin/Cytoxan (AC) followed by 30 days of radiation. Was 53 yrs old and did really well. Was able to work full time except for
Hello I was diagnosed in 2006 with BC in the right breast stage 11, lymph node involvement 4. Treatment lumpectomy, 6 cycles every 3 weeks of a cocktail of Taxotere and Adriamycin/Cytoxan (AC) followed by 30 days of radiation. Was 53 yrs old and did really well. Was able to work full time except for
Tobysasha65
in
SHARE Metastatic Breast Cancer
6 years ago
Adriamycin, Cytoxan Treatment
Hello! Everyone I'm going to my initial treatment tomorrow jan. 2, 2019 Happy New Year! 😊😁😂Any advice what to do after getting the infusion. Thanks all. I'm schedule to work the next day but my supervisor give me time to rest very thankful she's very supportive.
Hello! Everyone I'm going to my initial treatment tomorrow jan. 2, 2019 Happy New Year! 😊😁😂Any advice what to do after getting the infusion. Thanks all. I'm schedule to work the next day but my supervisor give me time to rest very thankful she's very supportive.
Angeloveme
in
SHARE Breast Cancer Support
6 years ago
No post for long time, here is my update.
For fellow Gleason 10 diagnoses. I found that when I was diagnosed I found it difficult to find any information about what I could expect. I know that none of us have the same reactions to the same medication but still I’ll list what I’ve be through so they might see what could transpire. I was diagnosed
For fellow Gleason 10 diagnoses. I found that when I was diagnosed I found it difficult to find any information about what I could expect. I know that none of us have the same reactions to the same medication but still I’ll list what I’ve be through so they might see what could transpire. I was diagnosed
Glsn10
in
Advanced Prostate Cancer
6 years ago
Oral Cytoxan and Avastin
Hi I have been on Cytoxan/Avastin for awhile now I get Avastin IV every 2 wks and take the Oral Pill every day. I have been noticing bad aches and pains. I guess it’s muscle/joint and even bone pain. Anyone else get this. It seems to be worse now . It’s mostly my hips and thigh. I’m also very stiff
Hi I have been on Cytoxan/Avastin for awhile now I get Avastin IV every 2 wks and take the Oral Pill every day. I have been noticing bad aches and pains. I guess it’s muscle/joint and even bone pain. Anyone else get this. It seems to be worse now . It’s mostly my hips and thigh. I’m also very stiff
Susansblessing
in
SHARE Ovarian Cancer Support
6 years ago
Any information
On 50 milligrams prednisone until 3 weeks ago. I had to take that amount but it made me feel horrible. I have been decreasing 10 mg weekly for the past 3 weeks. As of two days ago I am now on 20 mg a day with cytoxan every other month daily. When will I feel the decreased effect of taking prednisone
On 50 milligrams prednisone until 3 weeks ago. I had to take that amount but it made me feel horrible. I have been decreasing 10 mg weekly for the past 3 weeks. As of two days ago I am now on 20 mg a day with cytoxan every other month daily. When will I feel the decreased effect of taking prednisone
Hunter1234_
in
Vasculitis UK
6 years ago
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