Et: I have ET for 10 years been on interferon 2b... - MPN Voice

MPN Voice

10,445 members14,398 posts

Et

Jbut profile image
Jbut
5 Replies

I have ET for 10 years been on interferon 2b,been to hospital to pick meds up today and they said dont do 2b anymore,so my new med is interferon 2a any advice would be great ,does it do the same x

Written by
Jbut profile image
Jbut
To view profiles and participate in discussions please or .
Read more about...
5 Replies
swimswam profile image
swimswam

Hi jbut,

I have ET, and was on Intron (interferon alfa-2b) also told by my hospital two months ago it could no longer get supplies. I was given Roferon (interferon alfa-2a) instead and on phoning to check told it was the same thing. I have found no difference, just the fact that the Intron came in pen form and the Roferon is single injections. I don’t know whether it’s my technique but I find the longer needle slightly harder to inject and seems to bruise my stomach more, but other than that it seems no different, just made by a different company.

Malaika profile image
Malaika

Hi I have had the same happen to me. It does appear in my case to behave in the same way. I am to have an early blood test to see how it impacts my blood counts. It is a single injection and as I had no help it did give me some issues as not overly confident with this kind of application but went to see my nurse which reassured me and now I have no issues with the injection. Hope you manage it.

Best regards

Malaika

charl17 profile image
charl17

Maybe this helps. 6 months ago, when I started Pegasys they prescribed ridiculously large capacity syringes for me with long needles. I switched to over the counter half-ml insulin syringes with short narrow gauge needles. They work well and they are cheap. The low capacity makes it easier to extract the precise dose from the vial. It surprised me that the hematologists staff seemed to have so little practical experience with Pegasys injections. One-ml syringes are also available for higher doses. Diabetics do sub-q injections very frequently.

light profile image
light

Hi jbut, I am ET patient and I have been on Pegulated Intferon Apha 2 for 6 years now. Started with small dose of 45mc during slow transfer from Haydroxy, over few months and slow increase of dosage and decrease off hydroxy. Now I am on 135mc everywhere weeks. I found that it helps me to take injections in the evening. At 5pm I take paracetamol and at 6pm I take Peg injection. Sometime I have very bad side effects like very bad flue symptoms and could last for a few or longer days. Every time is a different reaction and timing as it could be few days after I take injection or week after for whole week, etc.. Reaction is always different from bad to less bad. I keep taking paracetamol to help me with the pain, fever, etc.. Apart of side effects Peg is managing my blood counts, platelets. So it is working for me. My last appointment I was told by my nurse and pharmacy that they are having problem obtaining Peg, but they found the way to supply me with Peg.

Good luck with your treatment on Peg.

Jbut profile image
Jbut

Had my first injection of interferon alpha 2a on sunday, done this myself hope i done it ok, its crazy i have been fine for 10 years with the 2b,didnt even think about my ET that much,now am back to worrying about the change in medication,if my bloods will be the same,if i will have any side affects. Thanks for all your advice x

You may also like...

ET

hydroxcycarbamide and 75 mg of clopidogrel . I would have gone with interferon but covid ruled that...

Et

Does anyone have tingling in arms and legs Diagnosed in January with ET Put on hydra and hydroxy....

ET

ET 12 years ago I am on hydroxyurea 2000mg a day I have been as well as expected but the last year...

ET

Hi everyone not been on for a while had my appointment today my Platelets are now on 735 only got up

ET

tell me, when you are put on Hydroxy why do you have to keep taking the medication. Why can't you...