Anyone here do FEC/FAC chemo? How about Neulesta side effects? Feeling anxious - please share!

Laura....
Hi Laura! I honestly am not sure what chemo combo that is...FEC/FAC. I have however, had Neulastin injections. Eight of them.

The only real side effect that I had from that was bone pain in my legs, starting about 36 hours after the injection.

I know that others here have had different and varied side effects from it and I'm sure that they will chime in. All in all though, it wasn't bad for me...well, relatively speaking..lol!

Hugs,
CR

MAJW said:

Neulasta
I had this after each chemo..I do believe it helped greatly in keeping my white blood cell count WAY UP and prevented me from getting any type of infection...the first one kicked my butt, muscle spasms and bone pain....that's the only time it did this...the rest did not have this effect..It was well worth it..
I wish you the best and I am with you in "the count down!"

I had Neulasta after TAC
Like the others, I had the bone pain and muscle aches--sort of like a really bad flu. They only lasted a couple of days and I used Ibuprophen. In my opinion, it was very worth taking. I got it after the first 5 rounds of TAC and my counts did so well that my onc. said let's try not getting the Neulasta after the last round--wound up in the hospital for 5 days with a neutropenic fever--not good. So, for me, getting the Neulasta was very beneficial.

Good luck with your treatment.

Hugs, Renee

For ME - Neulasta was easy -
For ME - Neulasta was easy - no pain at all. All it did to me was 2 hrs, almost to minute, after injection I went to sleep for 2 hrs. Tht defiinately isn't true for all but it was for ME.

Susan

Dee said:

Starting FEC next week
hi ya

Im getting almost the opposite to you!I start on Tuesday with 3 rounds FEC 3 weekly followed by 9, weekly Taxol...so as as right now dont have a lot of advice but I will let you know how I get on with FEC next Tuesday!!!

I also asked about the FEC and there are quite a few woman who have been through this type...Im sure they will send their wisdom,love and thoughts

Dee

No Neulasta side effects for me
I did feel like I had a mild flu about days 4-6, but it was the same the first 2 cycles of chemo (Taxotere and Cytoxin) without Neulasta and the last 2 with Neulasta. I dreaded the potential side effects, but really didn't have any. Now, I had every side effect imaginable and then some from the Taxotere . . .

We're all different.

Suzanne

I'm IBC too. And Dr. C is
I'm IBC too. And Dr. C is well respected in the IBC world, so you're in good hands. My cocktail was TAC, 6 rounds, with neupogin instead of neulasta. So I can't speak specifically to your cocktail.

But, my overall advice with side effects is talk with everyone if you're having trouble with them. By everyone I mean the nurses, oncologists, medical assistant, pharmacist, etc. Each of these professionals look at your case from a slightly different viewpoint and have learned different things in their day to day experiences.

For example, I learned from the pharmacist that claritin is recommended by the manufacturer for the bone pain associated with neupogin (I think neulasta too), my oncologist didn't know about that. The claratin worked, I didn't have to take viocodin, and my oncologist learned something.

I would also recommend that you get the specific names of the FEC/FAC and look them up. There are several very good sites that discuss the side effects of chemo drugs...sorry they're not coming to mind right now.

Also, if you do have trouble with a side effect, come back and ask here. Even if we haven't had your specific cocktail, we'll do our best to help you.

If the anxiety gets really bad, ask Dr. C for something to help with that. My onc prescribed atavan, told me to take it the night before and the morning of my first treatment, as needed after that.

Finally, know that you are strong enough to get through this. Just breathe and take one step at a time.

Hugs,

Linda

Hippiechick58 said:

Neulasta kicks my butt every
Neulasta kicks my butt every time! I just had injection # 7 of 8 total and boy am I looking forward to being done with this. I usually end up in bed for 4 or 5 days after injection. I take Celebrex and Oxycodone and it does help somewhat. I can imagine what the pain would be like without them!!

Remember, everyone is different so your experience might be quite different than mine (I hope)

Hang in there. You can do this.
Dianne

Celebrex/Neulasta

Just had my second chemo tx,TC, and my second Neulasta shot. Had no problems with either the first time, but today, I am experiencing so much pain. All the meds I was given were in reference to nausea. Did your doctor prescribe Celebrex right off the bat, or did you try Ibuprofen or Extra Strength Tylenol first? I'm assuming the combo of Celebrex and Neulasta are okay?? Since chemo's effecting all my organs, I don't want to do anything additional to make things worse. Thanks for any input you can provide.