Hi..There is no concrete data that taking Neup will have an effect of lowering platlets.,however there is significant data that the use of Neup is for the most part unnecessary for patients receiving HCV therapy.(you may be interested in the discussion here I linked below.
Having said that many doctors will prescribe it if the ANC(neutrophils drop down to approx. .5 . even given the data that says HCV therap patients having problems with bacterial infection is extremely rare.
Also Neup is not FDA approved for HCV therap patients ,it is used mainly for cancer patients todoing chemo -therapy..
What is your ANC ..you have not mentioned this?
Here is the discussion a number of months ago ,with significant data included:
http://www.medhelp.org/posts/Hepatitis-C/Some-clarification-if-someone-knows-or-doctor-has-explained/show/1656098?personal_page_id=1837989
Also here is some facts on Neup side effects :
Best to you..
Will
Cancer Patients Receiving Myelosuppressive Chemotherapy
In clinical trials involving over 350 patients receiving Neupogen® following nonmyeloablative cytotoxic chemotherapy‚ most adverse experiences were the sequelae of the underlying malignancy or cytotoxic chemotherapy. In all phase 2 and 3 trials‚ medullary bone pain‚ reported in 24% of patients‚ was the only consistently observed adverse reaction attributed to Neupogen® therapy. This bone pain was generally reported to be of mild-to-moderate severity‚ and could be controlled in most patients with non-narcotic analgesics; infrequently‚ bone pain was severe enough to require narcotic analgesics. Bone pain was reported more frequently in patients treated with higher doses (20 to 100 mcg/kg/day) administered IV‚ and less frequently in patients treated with lower SC doses of Neupogen® (3 to 10 mcg/kg/day).
In the randomized‚ double-blind‚ placebo-controlled trial of Neupogen® therapy following combination chemotherapy in patients (n = 207) with small cell lung cancer‚ the following adverse events were reported during blinded cycles of study medication (placebo or Neupogen® at 4 to 8 mcg/kg/day). Events are reported as exposure-adjusted since patients remained on double-blind Neupogen® a median of 3 cycles versus 1 cycle for placebo.
% of Blinded Cycles With Events
Event
Neupogen®
N = 384 Patient
Cycles
Placebo
N = 257 Patient
Cycles
Nausea/Vomiting
57
64
Skeletal Pain
22
11
Alopecia
18
27
Diarrhea
14
23
Neutropenic Fever
13
35
Mucositis
12
20
Fever
12
11
Fatigue
11
16
Anorexia
9
11
Dyspnea
9
11
Headache
7
9
Cough
6
8
Skin Rash
6
9
Chest Pain
5
6
Generalized Weakness
4
7
Sore Throat
4
9
Stomatitis
5
10
Constipation
5
10
Pain (Unspecified)
2
7
In this study‚ there were no serious‚ life-threatening‚ or fatal adverse reactions attributed to Neupogen® therapy. Specifically‚ there were no reports of flu-like symptoms‚ pleuritis‚ pericarditis‚ or other major systemic reactions to Neupogen®.
:http://www.drugs.com/sfx/neupogen-side-effects.html