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Pegasys
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Minimal Residual Disease or Cure in MPNs? Rationales and perspectives on Combo Therapy with Interferon-alpha2 and Ruxolitinib
Cutting edge therapy for PV - MF patients who do not respond to Jakafi or
Pegasys
alone - http://bit.ly/2tBjHVs
Cutting edge therapy for PV - MF patients who do not respond to Jakafi or
Pegasys
alone - http://bit.ly/2tBjHVs
PVReporter
in
MPN Voice
7 years ago
Good results today
Still pleased I chose to go with
Pegasys
and hoping it continues to work this well..!
Still pleased I chose to go with
Pegasys
and hoping it continues to work this well..!
AndyT
in
MPN Voice
7 years ago
Pegasys
Has anyone on
Pegasys
experienced any episodes of severe dizziness or fainting?
Has anyone on
Pegasys
experienced any episodes of severe dizziness or fainting?
HelenK
in
MPN Voice
7 years ago
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Anyone out there on PEGASYS Interferon ?
My question is
Pegasys
Interferon - whats it like to take ? Can anyone give me advice, tips, pointers in advance of September ? Thanks in advance...Jocko
My question is
Pegasys
Interferon - whats it like to take ? Can anyone give me advice, tips, pointers in advance of September ? Thanks in advance...Jocko
Jocko
in
MPN Voice
7 years ago
Change Hydroxycarbomide to Pegasys?
I was wondering if I changed to
Pegasys
would that stop the breathlessness. Has anybody got any advice before I see my consultant on Wednesday?
I was wondering if I changed to
Pegasys
would that stop the breathlessness. Has anybody got any advice before I see my consultant on Wednesday?
Anita53
in
MPN Voice
7 years ago
Pegasy
My consultant started me on
Pegasys
last Wednesday, i must admitted i felt fine until Sunday night and yesterday (monday) where i was having chills, hot sweats I felt like i had flu. I am taking
Pegasys
90mg/0.5ml. I have been dosing myself up on paracetamol.
My consultant started me on
Pegasys
last Wednesday, i must admitted i felt fine until Sunday night and yesterday (monday) where i was having chills, hot sweats I felt like i had flu. I am taking
Pegasys
90mg/0.5ml. I have been dosing myself up on paracetamol.
linphy
in
MPN Voice
7 years ago
Life with ET.
I've been on
Pegasys
(45mm every third week) for a good 3 years now. Lots of side effects, but bearable. Now I have "grown" some horrible pains in my feet. First I thought it was some sort of podagra, but it's not---most of the pain is located under my heels, so walking is pure torture.
I've been on
Pegasys
(45mm every third week) for a good 3 years now. Lots of side effects, but bearable. Now I have "grown" some horrible pains in my feet. First I thought it was some sort of podagra, but it's not---most of the pain is located under my heels, so walking is pure torture.
yarrowleaf
in
MPN Voice
7 years ago
Pegasys dosage
Hi, can anyone tell me the maximum dose for
Pegasys
? I've been on it several months with ever increasing doses as not getting any reduction in counts. Consultant today put the dose up to 270 per week. Is this ok? It seems a bit scary? Thanks, Frances.
Hi, can anyone tell me the maximum dose for
Pegasys
? I've been on it several months with ever increasing doses as not getting any reduction in counts. Consultant today put the dose up to 270 per week. Is this ok? It seems a bit scary? Thanks, Frances.
francesb
in
MPN Voice
7 years ago
Anagrelide and side effects
She said her colleague advised to commence
Pegasys
and it was NOT contraindicated in my case. She said she would apply for it and see me a month later.
She said her colleague advised to commence
Pegasys
and it was NOT contraindicated in my case. She said she would apply for it and see me a month later.
Dianne-Guisborough
in
MPN Voice
7 years ago
Does anyone have any info whether Interferon is contraindicated if you have a history of PE or other thrombolytic event ?
Also if anyone with a history of thrombolytic events is on
pegasys
interferon . I'm a proper awkward child ! -- Because of my history of melanoma I cannot have hydroxyurea. Any advice greatly appreciated Kind regards Dianne Xx
Also if anyone with a history of thrombolytic events is on
pegasys
interferon . I'm a proper awkward child ! -- Because of my history of melanoma I cannot have hydroxyurea. Any advice greatly appreciated Kind regards Dianne Xx
Dianne-Guisborough
in
MPN Voice
8 years ago
Platelets creeping back up - ET CALR+ve
Anyone else had experience of
Pegasys
or regular interferon becoming less effective over time..?
Anyone else had experience of
Pegasys
or regular interferon becoming less effective over time..?
AndyT
in
MPN Voice
8 years ago
KD
Hi everyone I was dx in 2014 with PV IM currently taking aspirin and getting phelbotomies, im curious is anyone taking the combo drug Rux (Jakifi) and
Pegasys
(IFN) I hear that they have been getting promising results with these 2 meds when taking together.
Hi everyone I was dx in 2014 with PV IM currently taking aspirin and getting phelbotomies, im curious is anyone taking the combo drug Rux (Jakifi) and
Pegasys
(IFN) I hear that they have been getting promising results with these 2 meds when taking together.
Hidden
in
MPN Voice
8 years ago
Reducing dosage of Pegasys
Hi, anyone got any experiences of reducing
pegasys
dosage? I was initially prescribed 45mcg once a week about a year ago. Platelets dropped quickly. For the past 4 months I have been taking 45mcg every 2 weeks.
Hi, anyone got any experiences of reducing
pegasys
dosage? I was initially prescribed 45mcg once a week about a year ago. Platelets dropped quickly. For the past 4 months I have been taking 45mcg every 2 weeks.
maryv
in
MPN Voice
8 years ago
Pegasys and hair loss???
Groan .. :-/ Has anyone had any experience of hair loss on
Pegasys
? Thank you, xx
Groan .. :-/ Has anyone had any experience of hair loss on
Pegasys
? Thank you, xx
Loubielou
in
MPN Voice
8 years ago
Eye Infection
I am recently diagnosed PV Jak2 and just started
Pegasys
on low dose weekly injection and Aspirin. Yesterday I woke with a very painful swollen eyelid and have had to go to GP for ointment. It seems to be a bit better this afternoon.
I am recently diagnosed PV Jak2 and just started
Pegasys
on low dose weekly injection and Aspirin. Yesterday I woke with a very painful swollen eyelid and have had to go to GP for ointment. It seems to be a bit better this afternoon.
Edgbastonian
in
MPN Voice
8 years ago
PV and I'm new here!
i have felt so go, but today started
Pegasys
and although been and felt so sick feeling better now.
i have felt so go, but today started
Pegasys
and although been and felt so sick feeling better now.
Lps1156
in
MPN Voice
8 years ago
Results of Pegasys Study
I've been on
Pegasys
since last October for my ET and am very pleased with it so far - fingers crossed..!
I've been on
Pegasys
since last October for my ET and am very pleased with it so far - fingers crossed..!
AndyT
in
MPN Voice
8 years ago
Pegasys - more good news
Their clinic now has 45 ET and PRV patients on
Pegasys
, with very good results and they are publishing their study findings at a haematology congress next week. I'll post the details on here once they are officially published.
Their clinic now has 45 ET and PRV patients on
Pegasys
, with very good results and they are publishing their study findings at a haematology congress next week. I'll post the details on here once they are officially published.
AndyT
in
MPN Voice
8 years ago
Pegasys 135
Hi has anybody got any lnformation on
pegasys
side afects lam on one injection per week thank you
Hi has anybody got any lnformation on
pegasys
side afects lam on one injection per week thank you
baggies
in
MPN Voice
9 years ago
Hydroxycarbamide v Pegasys Interferon
Hi I am due to start having treatment for PV, so far have just been having aspirin daily and venesections when needed. My haematological thinks it's time to start with treatment and I have been fortunate to have been offered the choice between the two. I am leaning towards interferon but am worried as
Hi I am due to start having treatment for PV, so far have just been having aspirin daily and venesections when needed. My haematological thinks it's time to start with treatment and I have been fortunate to have been offered the choice between the two. I am leaning towards interferon but am worried as
MicheleL
in
MPN Voice
9 years ago
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