HU and trigger finger: Hi everyone, I am so glad... - MPN Voice

MPN Voice

10,445 members14,398 posts

HU and trigger finger

digijools profile image
2 Replies

Hi everyone,

I am so glad my specialist recommended this group 4 years ago when i was diagnosed. You all have helped me so much.

I started on HU about 6 mos ago and now am developing trigger fingers in both my hands, middle fingers. I had this before with post partum thyroiditis 15 years ago. I had my thyroid checked and so far nothing. Could it be HU related?

No other real side effects to report.

Thanks in advance!

Written by
digijools profile image
digijools
To view profiles and participate in discussions please or .
2 Replies
hunter5582 profile image
hunter5582

Peripheral neuropathy is one of the listed side effects of HU, which may or may not be what you are experiencing. If so, this is a rare but serious adverse reaction to HU.

The WebMD site had one person who reported this same potential side effect webmd.com/drugs/drugreview-... . Perhaps this is a side effect that is so rare that it is just not reported. However, joint pain is listed by some sources as a potential side effect of HU mayoclinic.org/drugs-supple... .

If you are JAK2 positive, it would also be possible that this is inflammation related to the increased load of inflammatory cytokines you may be experiencing. HU does nothing to reduce this since that is not how it works.

I would definitely follow up on this. Per the NIH, HU is a "highly toxic medication with a low therapeutic index." While some people tolerate it without issues, it is pretty common to experience evidence of toxicity at therapeutic doses. Your prescriber needs to be aware of the potential toxicity you are experiencing. There are other options if HU won't work for you.

digijools profile image
digijools

Thanks hunter5582

You may also like...

HU to Peg Transition Problems -

generally feeling OK, I developed resistance to HU. A BMB in 2021 indicated I still had ET but now...

Symptom Relief. With HU

have Pv Jal2+ and just started HU about 3 weeks ago at 1000Mg 7 days a week. My question is anyone...

Pegasus, Hu and Iron

just started Pegasus as HU had not yet stabilised my bloods (after two years of increasing...

Switch from HU to Pegasys - update 4.0

week when I had my blood test (tested positive the following day and thought I just had a mild cold...

Does PV or taking HU cause gout

patients with PV or those taking HU developed gout? Thank you in advance for your advice.