Hep C Discussion Forum

Members Login
Username 
 
Password 
    Remember Me  
Chatbox
Please log in to join the chat!
Post Info TOPIC: Does procrit make you feel sick?


Senior Member

Status: Offline
Posts: 139
Date:
RE: Does procrit make you feel sick?
Permalink  
 


Had the first shot thursday and felt great all weekend.  Nice to get a few chores done.  Went in this AM for second shot and they said I was at 10.9 and didn't need another shot.



__________________

Hep C 1a since probably 1981.  Incivek, riba and interferon-48 weeks.  UND at weeks 2-4-6-8-10-12-16-20-24.  Previously Interferon alone for 6 months non-responder.  SVR 48 weeks 12/11/14



Guru

Status: Offline
Posts: 791
Date:
Permalink  
 

Malcolm, my voice of reason...you were right again ;-( it was just a fluctuation seems so...or AHCC has influence on Lymphocytes numbers only (still high lymphocytes compared to other blood test pre AHCC)

i just got call from lab...

WBCC - 2.4
Lymphocytes - 1.6
Neutrophiles - 0.5!!!! (thats a limit where i should stop with Interferon!)

it was a nice thing hoping/dreaming that just via OTC supplement things could improve. I got 9 shots more to go, seems i might consider obtaining Nupogen on my own again...

best



__________________

GT 3 dg. 08-2012 / FibroScan: 5 kPa F1 / FibroTest: F0-1 A1 / SoC TX: PegInt 120mcg+Riba 1000mg UND from w8 relapse EOT+4w
01-2016 Sof+Dac+Riba UND from w8, SVR24!




Guru

Status: Offline
Posts: 820
Date:
Permalink  
 

I didn't ask him, i told him i am stopping and he talked me into 1/2 dose 2x week. I was on the full 480 MCG 3x week. So we will see..He said a little high is way better than very low. I was at 2.0.



__________________

58 yo..Relapsed in 99 and again in 2004. Started triple therapy with Victrelis July 22,2012.  genotype 1a. week 8,12,16,24 VL Undetectable..E.O.T -- 6-22-2013,,,EOT + 24., UND. 

SVR !!!

 

~Bob~



Guru

Status: Offline
Posts: 3398
Date:
Permalink  
 

Hi Bob,

Those are seriously high WCC numbers. I would ask my doctor if I could stop the Neupogen. Cheers.



__________________

Geno 1b, IL28B CT,  x3 prior relapser,  ex-cirrhotic, 75 yo, did 48 weeks with Victrelis/Peg./Riba.  VL 1.28m at start, UNDET. at 8 ,12 ,16 ,24 ,30  and 48 weeks.  EOT 15 Feb 2013 , UNDET. at EOT + 28 weeks. SVR!  Still Undet. at EOT +5 years

Malcolm



Senior Member

Status: Offline
Posts: 139
Date:
Permalink  
 

Took my first shot this AM.  No side effects experienced.  Of course with all the other sx how would one notice.

blankstare



__________________

Hep C 1a since probably 1981.  Incivek, riba and interferon-48 weeks.  UND at weeks 2-4-6-8-10-12-16-20-24.  Previously Interferon alone for 6 months non-responder.  SVR 48 weeks 12/11/14



Guru

Status: Offline
Posts: 820
Date:
Permalink  
 

A little at first, i am only doing 1/2 shot 2x week. Tylenol takes it away.



__________________

58 yo..Relapsed in 99 and again in 2004. Started triple therapy with Victrelis July 22,2012.  genotype 1a. week 8,12,16,24 VL Undetectable..E.O.T -- 6-22-2013,,,EOT + 24., UND. 

SVR !!!

 

~Bob~



Guru

Status: Offline
Posts: 791
Date:
Permalink  
 

wow 13.4! ;-D WBC thru the roof ;-D

u feel any sx from Nupogen? (bone pain?)



__________________

GT 3 dg. 08-2012 / FibroScan: 5 kPa F1 / FibroTest: F0-1 A1 / SoC TX: PegInt 120mcg+Riba 1000mg UND from w8 relapse EOT+4w
01-2016 Sof+Dac+Riba UND from w8, SVR24!




Guru

Status: Offline
Posts: 820
Date:
Permalink  
 

you love blood charts, here is mine from yesterday, with neupogen..

Capture.JPG



Attachments
__________________

58 yo..Relapsed in 99 and again in 2004. Started triple therapy with Victrelis July 22,2012.  genotype 1a. week 8,12,16,24 VL Undetectable..E.O.T -- 6-22-2013,,,EOT + 24., UND. 

SVR !!!

 

~Bob~



Guru

Status: Offline
Posts: 791
Date:
Permalink  
 

some interesting publications re AHCC:

http://www.ncbi.nlm.nih.gov/pubmed/23351405

http://www.ncbi.nlm.nih.gov/pubmed/19827270

http://www.ncbi.nlm.nih.gov/pubmed/18752476

http://www.ncbi.nlm.nih.gov/pubmed/18304499

http://www.ncbi.nlm.nih.gov/pubmed/17555784

i smell it really might have some immunomodulation properties...maybe not as much as marketed by some, but then again it might not be snake oil ;-D

cheers



__________________

GT 3 dg. 08-2012 / FibroScan: 5 kPa F1 / FibroTest: F0-1 A1 / SoC TX: PegInt 120mcg+Riba 1000mg UND from w8 relapse EOT+4w
01-2016 Sof+Dac+Riba UND from w8, SVR24!




Guru

Status: Offline
Posts: 791
Date:
Permalink  
 

I love charts too

i am obligated (doc orders) to have blood test every 2 weeks (i did few 3 weeks apart), i only did one week after another last time when neutrophiles dropped to 0.7 (and total WBC to 2.1)...doc said although @ 0.7 neutrophiles i am supposed to get 50% lower dose of interferon, she wanted to wait also for WBC to drop to 1.75 to do it.

please notice lymphocytes levels...pre tx level 1.9 > tx > 1.7 > 1.3 > 1.2 > 1 week of ahcc > 2.0? this kinda makes me think it's not a fluke...if it is i will gladly stop with AHCC and save me 300$ monthly

can't wait for tomorrow's blood check to add to this chart and check how it is correlating. Also soon i will get PCR results (12th week)

i would love to check my vitamin levels (i only did Vit D 2 months ago, it's was high normal range), but each one is 30$ and it take minimum 2 weeks (at least at this private lab i am going to) Would love to know shall i stop or add some as vitamins as supplements. I would definetly do B12/B9, Vit E and Vit A.

as i said, i don't trust any "magical supplements", but seems lots of oncologists are into AHCC supplementation? there must be something in it then...if it really works, i feel it's my duty to share my experience to my fellow hcv friends on this forum, since i know lots of em have issues with wbc and going for Nupogen to help...

again you are my voice of reason

hows your recovery going? you got some new results? (PCR, blood check)? Are you taking some particular diet in those crucial 12-24w EOT?

all the best



__________________

GT 3 dg. 08-2012 / FibroScan: 5 kPa F1 / FibroTest: F0-1 A1 / SoC TX: PegInt 120mcg+Riba 1000mg UND from w8 relapse EOT+4w
01-2016 Sof+Dac+Riba UND from w8, SVR24!




Guru

Status: Offline
Posts: 3398
Date:
Permalink  
 

Hi Zlikster,

You know I love looking at blood charts. Just to show normal fluctuations, here are my WCC and Neutrophils from week 24 to week 37.

28.8.12    WCC: 2.7     Neutrophils: 1.16

12.9.12    WCC  2.4     Neut.          0.80

9.10.12    WCC  2.5     Neut.          1.15

28.11.12  WCC: 3.1     Neut.          1.54

I took no supplements at all, and had stopped Vit D at that stage as my blood levels were high-normal.

If you look at your results, you will see that everything was low on 11.04.13, including your Hb. On 19.4.13, they had all gone back up. Such fluctuations are normal, and by having blood tests so often, you'll drive yourself nuts.

Sorry about the AHCC. After reading your post, I saw it in my local Pharmacy, and asked the Chemist to look it up, as I had never heard of it. Quote: 'it induces a feeling of wellbeing and gently massages the immune system'.  He said he sells some to young Asian girls who attend the nearby English Language College. If you believe it helps, go for it. Cheers.



__________________

Geno 1b, IL28B CT,  x3 prior relapser,  ex-cirrhotic, 75 yo, did 48 weeks with Victrelis/Peg./Riba.  VL 1.28m at start, UNDET. at 8 ,12 ,16 ,24 ,30  and 48 weeks.  EOT 15 Feb 2013 , UNDET. at EOT + 28 weeks. SVR!  Still Undet. at EOT +5 years

Malcolm



Guru

Status: Offline
Posts: 791
Date:
Permalink  
 

Omega3+Vit E capsule, Vitamin C, B12 and Folacin - approved by doc, nada helped raise WBC tho, i started to take B12 on 2nd month of therapy when neutrophiles dropped to 1.2 (first pills 2x500, then one im injection, no raise in WBC, they went lower!)

Vitamin D i am taking cause of my fracture bone issue (i have stopped with calcium citrate tho), i am making a pause with it now (sunny days!)

i know  WBC can go up n down on it's own, but looking at my blood test, i never had from start of therapy a raise in WBC, only constant drops and as i said, i am not gonna jump to conclusion from one positive blood test, but in just 1 week of taking AHCC (and folic acid) such a dramatic increase looks strange...please take a look at my blood test chart.




as for AHCC, i am not a "beliver" in it. I am all for scientifically approved supplements and medicines, i do not buy "snake oils",am appaled by homeopathic schenanigans,etc as i mentioned this is a tip from a guy who was recommended ahcc by his oncologist (seems oncologists do tend to recommend ahcc supplement) when his WBC went seriously down from 3xinterferon shots weekly therapy....i was desperate to bring neutrophiles up, since i really didn't wanna stop or lower dosage of interferon half way there and my hepa was about to lower interferon dosage by 1/3 then 1/2 and even considering a pause...as for Nupogena, my hepa said it's not easy to obtain and she is worried about it's sx too (i was about to find it on my own).

Getting blood drawn on Friday, can't wait to see WBC situation. If WBC will be even higher then 2 weeks ago, then i will have to jump to conclusion - AHCC works definetly in raising WBC...and i am more willing to spread this tip to all people that have WBC issues cause of interferon sx, before opting in for Nupogena. Maybe it is individual response to AHCC? not sure, in any way i am really thankful for a guy that gave me this tip (well, and his oncologist)...from what i have seen in articles on AHCC it gives a huge boost to lymphocytes production (take a look and my Lymphocytes numbers please!), which is kinda what i have seen from last blood test.

i am paying 45$ for 30 capsules (500mg) and i am taking daily 3x2, so it is expensive, there are cheaper brands (a LOT cheaper), but guy that gave me this tip told me to go for immunomax one only.

all the best. i am really keen on your opinion Malcolm! please check my blood stats...




__________________

GT 3 dg. 08-2012 / FibroScan: 5 kPa F1 / FibroTest: F0-1 A1 / SoC TX: PegInt 120mcg+Riba 1000mg UND from w8 relapse EOT+4w
01-2016 Sof+Dac+Riba UND from w8, SVR24!




Guru

Status: Offline
Posts: 3398
Date:
Permalink  
 

Hi Zikster,

By all means keep taking your AHCC if you want to. Unfortunately it has no effect on WBC production. It's a mushroom extract from Japan which supposedly 'stimulates' your immune system, and you can buy it here, at  A$15.99 for 50 capsules ( that has Immunomax on the label). Your Vitamin intake is impressive- has your Doctor approved all of those?  Remember your WBC can go up and down on their own- also if you are dehydrated when you have your blood test, your counts will be a bit higher. Cheers.



__________________

Geno 1b, IL28B CT,  x3 prior relapser,  ex-cirrhotic, 75 yo, did 48 weeks with Victrelis/Peg./Riba.  VL 1.28m at start, UNDET. at 8 ,12 ,16 ,24 ,30  and 48 weeks.  EOT 15 Feb 2013 , UNDET. at EOT + 28 weeks. SVR!  Still Undet. at EOT +5 years

Malcolm



Senior Member

Status: Offline
Posts: 139
Date:
Permalink  
 

I was just informed that I need to start taking shots 2x per week.  Not sure for how long though.  Thanks for the information.



__________________

Hep C 1a since probably 1981.  Incivek, riba and interferon-48 weeks.  UND at weeks 2-4-6-8-10-12-16-20-24.  Previously Interferon alone for 6 months non-responder.  SVR 48 weeks 12/11/14



Guru

Status: Offline
Posts: 791
Date:
Permalink  
 

strange, can't find any USA site that sells this particular brand, most of em are in EU. It's an OTC supplement, tho in my local pharmacy they sell 2 kinds: immunomax ahcc and some other with smaller amount of ahcc (apparently with same extract) but 10 times cheaper, tho for that cheaper one guy who told me about this supplements and  it's WBC influence, said it's no good. His onccologist recommended it while he was on 3 interferon shots per week for lymph cancer. My doc (hepa) doesn't belives in it at all. To be honest i don't trust supplements marketed with some questionable and sometimes "magical" claims, but if it is the thing that raised my wbc and it's completley safe with no sz, then i don't care what marketing or doctors say

http://www.ebay.com/sch/i.html?_trksid=p2050601.m570.l1313.TR10.TRC1&_nkw=ahcc&_sacat=0&_from=R40 there are plenty of AHCC supplements, but no Immunomax one (maker is from Finland i think)...not sure is it all same or doctors are just pushing expensive cause of manufacturer lobbying em.

can't wait for friday and blood results to be honest, from all supplements (omega3, Vit E, Vit D, Vit C, B12) there was no change in blood cell counts, until this one, tho i did added another supplement with ahcc too, folic acid (B9, one pill daily).



__________________

GT 3 dg. 08-2012 / FibroScan: 5 kPa F1 / FibroTest: F0-1 A1 / SoC TX: PegInt 120mcg+Riba 1000mg UND from w8 relapse EOT+4w
01-2016 Sof+Dac+Riba UND from w8, SVR24!




Guru

Status: Offline
Posts: 820
Date:
Permalink  
 

They don't sell that here..Just looked it up.



__________________

58 yo..Relapsed in 99 and again in 2004. Started triple therapy with Victrelis July 22,2012.  genotype 1a. week 8,12,16,24 VL Undetectable..E.O.T -- 6-22-2013,,,EOT + 24., UND. 

SVR !!!

 

~Bob~



Guru

Status: Offline
Posts: 791
Date:
Permalink  
 

i just want to say that i might had a lucky way of recovering neutrohiles/wbc in 7 days from just one supplement. My doc doesn't belives me, but i haven't been taking anything else.

ImmunoMax AHCC (3x2 tabs daily), after a week neutrophiles from 0.7 went to 1.1, wbc from 2.1 to 3.5. Now it might be a fluke (i doubt it's a placebo fx), but it was first raise in wbc since therapy started. I am gonna get another blood test on Fri and see are they up even more (continued to drink ahcc)?

just a thought, before u opt in for Neupogen.



__________________

GT 3 dg. 08-2012 / FibroScan: 5 kPa F1 / FibroTest: F0-1 A1 / SoC TX: PegInt 120mcg+Riba 1000mg UND from w8 relapse EOT+4w
01-2016 Sof+Dac+Riba UND from w8, SVR24!




Guru

Status: Offline
Posts: 820
Date:
Permalink  
 

I had to start Neupogen also a couple weeks ago, a shot 2x week. No side effects, some people it hurts there bones. But tylenol or ibuprofin takes care of that. Weekly blood test too.



__________________

58 yo..Relapsed in 99 and again in 2004. Started triple therapy with Victrelis July 22,2012.  genotype 1a. week 8,12,16,24 VL Undetectable..E.O.T -- 6-22-2013,,,EOT + 24., UND. 

SVR !!!

 

~Bob~

DJ


Senior Member

Status: Offline
Posts: 306
Date:
Permalink  
 

Actually, I guess what I got is called Neupogen. I just got back from getting the injection. So far so good. She said hopefully I only need this one but we will see. I have to get a blood test test week to see if it worked. But she said that most who take Neupogen do not have side effects and that it should help me feel better (which would be nice to have more energy).

__________________

Genotype 3.  Treatment started on 1/11/2013 with Ribavirin and Pegatron.  Week 4 UND.  Week 12 UND.  Ended treatment on 6/28/2013.  Six months post treatment 12/04/2013 SVR.



Senior Member

Status: Offline
Posts: 227
Date:
Permalink  
 

I get a shot of it at the doctors office on the average once every two weeks. It stings lol. I haven't noticed being sick afterwards.
Within a few days after the first shot I felt a lot better. Sadly since then I haven't noticed such a substantial difference.
I do notice when I need it...though.

Hope it gets better for you!

__________________

GT 1a Started triple tx with Incivek, Pegasys, and Riba 2-6-2013. UND at 4,6,12,23,& 24 wks EOT 7-26-2013. Probably had Hep C for 20-30 years. Don't really know when I got it.



Senior Member

Status: Offline
Posts: 165
Date:
Permalink  
 

I have to get it too dj

__________________

Genotype 1a

1/18/13 -  VL 1.5mil triple therapy with boceprevir

2/3/14 - relapsed. 1.7ml

 

6/28/14 - started solvadi interferon and ribavirin for 12 weeks

7/28/14 - week 4 undetected dosage reduction of rib and peg

 

11/2/14 und 4 weeks post eot

 

g

 

DJ


Senior Member

Status: Offline
Posts: 306
Date:
Permalink  
 

Well I just got a call to go in the doctor's office this afternoon to get one of these shots. They are hoping I will only need one. I don't want to take it cause I don't really feel too bad and I am afraid it will make me sick. But I guess I have to. Hopefully it won't be too bad.

__________________

Genotype 3.  Treatment started on 1/11/2013 with Ribavirin and Pegatron.  Week 4 UND.  Week 12 UND.  Ended treatment on 6/28/2013.  Six months post treatment 12/04/2013 SVR.



Senior Member

Status: Offline
Posts: 118
Date:
Permalink  
 

Is Eprex the same as procrit? If so the box does say Flu like symptoms. I have been doing the Eprex for 8 weeks now ,1 a week and I find I vomit a lot more if I do anything that uses my energy pool up. I do feel a whole lot better now other than the vomiting.



__________________

Don't sweat the small stuff, it will only give you hair loss.

KLG


Veteran Member

Status: Offline
Posts: 76
Date:
Permalink  
 

Btw - no problem with my second procrit shot. Yay!

__________________

Geno 3a, stage 3, IL28 cc, diagnosed 94, interferon 1year, relapsed immediately, started RIBA/int on 2/1/13, 4 wk und. Female, age 55, EOT 7/18/13. 4 weeks UND, 12 weeks UND, 6 months UND!!!

KLG


Veteran Member

Status: Offline
Posts: 76
Date:
Permalink  
 

Congrats Ted on the und!!!

__________________

Geno 3a, stage 3, IL28 cc, diagnosed 94, interferon 1year, relapsed immediately, started RIBA/int on 2/1/13, 4 wk und. Female, age 55, EOT 7/18/13. 4 weeks UND, 12 weeks UND, 6 months UND!!!

KLG


Veteran Member

Status: Offline
Posts: 76
Date:
Permalink  
 

Thanks for the heads up about the insomnia. I will try procrit again in the afternoon and see what happens. For me, the interfuron doesn't seem as bad as all the RIBA problems!

__________________

Geno 3a, stage 3, IL28 cc, diagnosed 94, interferon 1year, relapsed immediately, started RIBA/int on 2/1/13, 4 wk und. Female, age 55, EOT 7/18/13. 4 weeks UND, 12 weeks UND, 6 months UND!!!



Member

Status: Offline
Posts: 27
Date:
Permalink  
 

I had to use procrit for six weeks(6 doses) made my joints ache,and did not sleep that good. It did do the job by brining my cell counts up.

 No way did I get as sick as enterfuron shots,everyone is different. KLT,after reading some of your posts,it sounds like your treatment is going alot like mine did. My  red blood cell count went way down so they transfused me...2 units, then got inemic turned white as a gohst, then platelets droped way down- 8.000,another transfusion.6 units,had every side affect in the book. however after 12 weeks,I went nondetectable,they stoped treatment  at week 12, that was 4 months ago and am still nondetec. not concidered healed yet But i feel great, so hang in there,it will be over soon and it will be worth it.

          -----TED



__________________

Ted...HCV genotype 1 cirrhosis stage 4  PEG,RIBA,INCEVEK taken off treatment after 20 weeks,low platelets,playing the waiting game..



Guru

Status: Offline
Posts: 592
Date:
Permalink  
 

Careful about taking it at night--caused me some insomnia and ended up using in the am so I could sleep--made for a really crappy day

__________________

Diagnosed 1996 genotype 1b VL alot tx starting 12/23/11 Victrelis UND week 8!!! 28 weeks of tx

Completed tx 7/6/12--still UND!!!!



Veteran Member

Status: Offline
Posts: 72
Date:
Permalink  
 

I used it for a month with no ill sx, and felt a lot better in one week. Still have 4 bottles in the cooler, feel like I could use it again at week 36:)



__________________

58yr m/G 1A/ VL 9,000,000 / F 3  / STARTED TRIPPLE TX (Incivek)7-14-12 / UND WK-4-8-12-16-20-24-36- 48- 12 weeks post tx UND. SVR 1-10-14

KLG


Veteran Member

Status: Offline
Posts: 76
Date:
Permalink  
 

Thanks! I was not expecting that! I only have to take it once a week and next time I will take it at bedtime rather than the afternoon. Ugh...

__________________

Geno 3a, stage 3, IL28 cc, diagnosed 94, interferon 1year, relapsed immediately, started RIBA/int on 2/1/13, 4 wk und. Female, age 55, EOT 7/18/13. 4 weeks UND, 12 weeks UND, 6 months UND!!!



Guru

Status: Offline
Posts: 592
Date:
Permalink  
 

Procrit made me feel really bad--pain in my feet & ankles and a genrally achiness all over and just sick. Some weeks it was better!

__________________

Diagnosed 1996 genotype 1b VL alot tx starting 12/23/11 Victrelis UND week 8!!! 28 weeks of tx

Completed tx 7/6/12--still UND!!!!



Veteran Member

Status: Offline
Posts: 62
Date:
Permalink  
 

It made me feel very sick. I just came off of it a few weeks ago. 



__________________

1b, 3rd time around on treatment. Stage IV cirr. Undetectable at 8 weeks with Incviek. Been infected since the late 70s. 48wk treatment completed. Sustained undetectable. 

KLG


Veteran Member

Status: Offline
Posts: 76
Date:
Permalink  
 

I took my first procrit shot a few hours ago. I am so sick, feel worse than interfuron shot... Is it just coincidental and maybe I just caught the flu?

__________________

Geno 3a, stage 3, IL28 cc, diagnosed 94, interferon 1year, relapsed immediately, started RIBA/int on 2/1/13, 4 wk und. Female, age 55, EOT 7/18/13. 4 weeks UND, 12 weeks UND, 6 months UND!!!

Page 1 of 1  sorted by
 
Quick Reply

Please log in to post quick replies.

Legal Disclaimer:

THIS FORUM, IT'S OWNERS, ADMINISTRATORS, MODERATORS AND MEMBERS DO NOT AT ANY TIME GIVE MEDICAL ADVICE AND IN ALL CASES REFER ANYONE HERE TO SEEK APPROPRIATE MEDICAL ADVICE FROM THEIR DOCTOR.