: utf-8

: January 29 2010 09:24:13.
:

words q 1 (max 200)words q 2 (max 200)words q 3 (max 200)
patients : 3.77 %
Aranesp : 3.14 %
ESAs : 2.09 %
anemia : 1.88 %
clinical : 1.67 %
events : 1.26 %
CRF : 1.26 %
receiving : 1.26 %
not : 1.26 %
chemotherapy : 1.05 %
risks : 1.05 %
site : 1.05 %
trials : 1.05 %
studies : 1.05 %
indicated : 1.05 %
reported : 1.05 %
hemoglobin : 1.05 %
other : 1.05 %
treatment : 0.84 %
serious : 0.84 %
cardiovascular : 0.84 %
visit : 0.84 %
use : 0.84 %
due : 0.84 %
myelosuppressive : 0.84 %
Anemia : 0.84 %
been : 0.84 %
cell : 0.84 %
rsaquo : 0.84 %
administered : 0.63 %
stroke : 0.63 %
greater : 0.63 %
agents : 0.63 %
therapy : 0.63 %
survival : 0.63 %
has : 0.63 %
death : 0.63 %
red : 0.63 %
have : 0.63 %
concomitant : 0.63 %
Chemotherapy : 0.63 %
should : 0.63 %
Chronic : 0.63 %
Failure : 0.63 %
risk : 0.63 %
Patients : 0.63 %
levels : 0.63 %
failure : 0.63 %
were : 0.42 %
overall : 0.42 %
Amgen : 0.42 %
cure : 0.42 %
controlled : 0.42 %
most : 0.42 %
side : 0.42 %
anticipated : 0.42 %
antibodies : 0.42 %
commonly : 0.42 %
outcome : 0.42 %
effects : 0.42 %
INCREASED : 0.42 %
hypertension : 0.42 %
participating : 0.42 %
only : 0.42 %
increased : 0.42 %
erythropoiesis-stimulating : 0.42 %
above : 0.42 %
response : 0.42 %
PRCA : 0.42 %
com : 0.42 %
WARNINGS : 0.42 %
EVENTS : 0.42 %
experienced : 0.42 %
severe : 0.42 %
fatigue : 0.42 %
target : 0.42 %
blood : 0.42 %
dialysis : 0.42 %
Use : 0.42 %
Information : 0.42 %
mortality : 0.42 %
including : 0.42 %
renal : 0.42 %
Cancer : 0.42 %
associated : 0.42 %
Renal : 0.42 %
chronic : 0.42 %
progression-free : 0.42 %
that : 0.42 %
Nonmyeloid : 0.21 %
without : 0.21 %
cytopenias : 0.21 %
neutralizing : 0.21 %
Malignancies : 0.21 %
aplasia : 0.21 %
contribute : 0.21 %
Cases : 0.21 %
pure : 0.21 %
reserved : 0.21 %
rights : 0.21 %
subcutaneous : 0.21 %
administration : 0.21 %
also : 0.21 %
predominantly : 0.21 %
treated : 0.21 %
Concomitant : 0.21 %
erythropoietin : 0.21 %
All : 0.21 %
weeks : 0.21 %
over : 0.21 %
Kidney : 0.21 %
cancer : 0.21 %
included : 0.21 %
than : 0.21 %
even : 0.21 %
insufficient : 0.21 %
While : 0.21 %
ESA : 0.21 %
myocardial : 0.21 %
infarction : 0.21 %
thrombosis : 0.21 %
rate : 0.21 %
rise : 0.21 %
access : 0.21 %
vascular : 0.21 %
congestive : 0.21 %
heart : 0.21 %
hemodialysis : 0.21 %
Map : 0.21 %
Site : 0.21 %
cross-react : 0.21 %
Seizures : 0.21 %
occurred : 0.21 %
Terms : 0.21 %
switched : 0.21 %
antibody-mediated : 0.21 %
withhold : 0.21 %
permanently : 0.21 %
discontinued : 0.21 %
Statement : 0.21 %
Privacy : 0.21 %
spasm : 0.21 %
edema : 0.21 %
vomiting : 0.21 %
muscle : 0.21 %
hypotension : 0.21 %
diarrhea : 0.21 %
Product : 0.21 %
infection : 0.21 %
suspected : 0.21 %
antibody-associated : 0.21 %
interferon : 0.21 %
Receiving : 0.21 %
ribavirin : 0.21 %
hepatitis : 0.21 %
undergoing : 0.21 %
alfa : 0.21 %
while : 0.21 %
Full : 0.21 %
sudden : 0.21 %
loss : 0.21 %
fever : 0.21 %
evaluated : 0.21 %
anti-erythropoietin : 0.21 %
count : 0.21 %
reticulocyte : 0.21 %
dyspnea : 0.21 %
accompanied : 0.21 %
low : 0.21 %
nausea : 0.21 %
completion : 0.21 %
malignancies : 0.21 %
non-myeloid : 0.21 %
MORTALITY : 0.21 %
SERIOUS : 0.21 %
Boxed : 0.21 %
Safety : 0.21 %
patient : 0.21 %
well-being : 0.21 %
Important : 0.21 %
CARDIOVASCULAR : 0.21 %
metastatic : 0.21 %
RECURRENCE : 0.21 %
transfusions : 0.21 %
need : 0.21 %
reduction : 0.21 %
PROGRESSION : 0.21 %
TUMOR : 0.21 %
THROMBOEMBOLIC : 0.21 %
STROKE : 0.21 %
RISK : 0.21 %
Studies : 0.21 %
life : 0.21 %
ongoing : 0.21 %
recurrence-free : 0.21 %
absence : 0.21 %
adequately : 0.21 %
hormonal : 0.21 %
therapeutic : 0.21 %
clinical trials : 0.99 %
patients receiving : 0.8 %
g dL : 0.8 %
cardiovascular events : 0.8 %
visit site : 0.8 %
rsaquo visit : 0.8 %
anemia due : 0.6 %
treatment anemia : 0.6 %
other ESAs : 0.6 %
risks death : 0.6 %
not indicated : 0.6 %
hemoglobin levels : 0.6 %
serious cardiovascular : 0.6 %
death serious : 0.6 %
patients CRF : 0.6 %
trials patients : 0.6 %
clinical studies : 0.6 %
been reported : 0.6 %
site Anemia : 0.6 %
myelosuppressive therapy : 0.4 %
therapy anticipated : 0.4 %
red blood : 0.4 %
receiving myelosuppressive : 0.4 %
indicated patients : 0.4 %
anticipated outcome : 0.4 %
blood cell : 0.4 %
studies that : 0.4 %
experienced greater : 0.4 %
commonly reported : 0.4 %
Aranesp other : 0.4 %
greater risks : 0.4 %
myelosuppressive chemotherapy : 0.4 %
outcome cure : 0.4 %
reported patients : 0.4 %
dL above : 0.4 %
ESAs target : 0.4 %
due concomitant : 0.4 %
levels g : 0.4 %
target hemoglobin : 0.4 %
Aranesp not : 0.4 %
should be : 0.4 %
agents ESAs : 0.4 %
events stroke : 0.4 %
Anemia Chronic : 0.4 %
stroke administered : 0.4 %
administered erythropoiesis-stimulating : 0.4 %
erythropoiesis-stimulating agents : 0.4 %
concomitant myelosuppressive : 0.4 %
most commonly : 0.4 %
Aranesp indicated : 0.4 %
reported side : 0.4 %
Renal Failure : 0.4 %
chronic renal : 0.4 %
overall survival : 0.4 %
severe anemia : 0.4 %
CRF participating : 0.4 %
receiving ESAs : 0.4 %
Failure rsaquo : 0.4 %
controlled clinical : 0.4 %
renal failure : 0.4 %
indicated treatment : 0.4 %
effects clinical : 0.4 %
studies patients : 0.4 %
failure CRF : 0.4 %
side effects : 0.4 %
Chronic Renal : 0.4 %
antibodies erythropoietin : 0.2 %
anemia or : 0.2 %
aplasia PRCA : 0.2 %
PRCA severe : 0.2 %
dL over : 0.2 %
cell aplasia : 0.2 %
without other : 0.2 %
or without : 0.2 %
Cases pure : 0.2 %
cytopenias associated : 0.2 %
other cytopenias : 0.2 %
contribute risks : 0.2 %
weeks contribute : 0.2 %
over weeks : 0.2 %
associated neutralizing : 0.2 %
pure red : 0.2 %
risks Cases : 0.2 %
neutralizing antibodies : 0.2 %
red cell : 0.2 %
stroke congestive : 0.2 %
insufficient hemoglobin : 0.2 %
hemoglobin response : 0.2 %
CRF insufficient : 0.2 %
Patients CRF : 0.2 %
above Patients : 0.2 %
response ESA : 0.2 %
ESA therapy : 0.2 %
greater risk : 0.2 %
even greater : 0.2 %
be even : 0.2 %
therapy be : 0.2 %
studies experienced : 0.2 %
participating clinical : 0.2 %
chemotherapy course : 0.2 %
course Aranesp : 0.2 %
completion chemotherapy : 0.2 %
following completion : 0.2 %
Discontinue following : 0.2 %
Aranesp contraindicated : 0.2 %
contraindicated patients : 0.2 %
Patients chronic : 0.2 %
hypertension Patients : 0.2 %
uncontrolled hypertension : 0.2 %
patients uncontrolled : 0.2 %
risk cardiovascular : 0.2 %
events mortality : 0.2 %
heart failure : 0.2 %
failure hemodialysis : 0.2 %
congestive heart : 0.2 %
erythropoietin have : 0.2 %
infarction stroke : 0.2 %
hemodialysis vascular : 0.2 %
vascular access : 0.2 %
hemoglobin rise : 0.2 %
rate hemoglobin : 0.2 %
thrombosis rate : 0.2 %
access thrombosis : 0.2 %
myocardial infarction : 0.2 %
included myocardial : 0.2 %
patients Aranesp : 0.2 %
other patients : 0.2 %
than other : 0.2 %
mortality than : 0.2 %
ESAs increased : 0.2 %
increased risks : 0.2 %
events included : 0.2 %
cancer events : 0.2 %
patients cancer : 0.2 %
events controlled : 0.2 %
rise g : 0.2 %
also been : 0.2 %
CRF were : 0.2 %
trials most : 0.2 %
Aranesp clinical : 0.2 %
participating Aranesp : 0.2 %
were infection : 0.2 %
infection hypertension : 0.2 %
spasm most : 0.2 %
muscle spasm : 0.2 %
hypotension muscle : 0.2 %
hypertension hypotension : 0.2 %
occurred patients : 0.2 %
have occurred : 0.2 %
be switched : 0.2 %
not be : 0.2 %
should not : 0.2 %
Patients should : 0.2 %
switched other : 0.2 %
ESAs as : 0.2 %
Seizures have : 0.2 %
cross-react Seizures : 0.2 %
antibodies cross-react : 0.2 %
as antibodies : 0.2 %
patients anemia : 0.2 %
concomitant chemotherapy : 0.2 %
Amgen All : 0.2 %
Map Amgen : 0.2 %
Site Map : 0.2 %
com Site : 0.2 %
All rights : 0.2 %
rights reserved : 0.2 %
US only : 0.2 %
use US : 0.2 %
site use : 0.2 %
reserved site : 0.2 %
Chemotherapy com : 0.2 %
com Chemotherapy : 0.2 %
edema nausea : 0.2 %
fatigue edema : 0.2 %
were fatigue : 0.2 %
chemotherapy were : 0.2 %
nausea vomiting : 0.2 %
vomiting diarrhea : 0.2 %
Amgen com : 0.2 %
dyspnea Amgen : 0.2 %
fever dyspnea : 0.2 %
diarrhea fever : 0.2 %
anemia Patients : 0.2 %
antibody-mediated anemia : 0.2 %
while undergoing : 0.2 %
ESAs while : 0.2 %
cure Discontinue : 0.2 %
has also : 0.2 %
undergoing treatment : 0.2 %
treatment hepatitis : 0.2 %
ribavirin sudden : 0.2 %
interferon ribavirin : 0.2 %
C interferon : 0.2 %
hepatitis C : 0.2 %
PRCA has : 0.2 %
administration PRCA : 0.2 %
has been : 0.2 %
Aranesp has : 0.2 %
rsaquo visit site : 0.8 %
visit site Anemia : 0.6 %
clinical trials patients : 0.6 %
risks death serious : 0.6 %
death serious cardiovascular : 0.6 %
serious cardiovascular events : 0.6 %
target hemoglobin levels : 0.4 %
erythropoiesis-stimulating agents ESAs : 0.4 %
ESAs target hemoglobin : 0.4 %
hemoglobin levels g : 0.4 %
agents ESAs target : 0.4 %
g dL above : 0.4 %
reported side effects : 0.4 %
side effects clinical : 0.4 %
renal failure CRF : 0.4 %
chronic renal failure : 0.4 %
commonly reported side : 0.4 %
most commonly reported : 0.4 %
administered erythropoiesis-stimulating agents : 0.4 %
Aranesp other ESAs : 0.4 %
treatment anemia due : 0.4 %
levels g dL : 0.4 %
Aranesp not indicated : 0.4 %
myelosuppressive therapy anticipated : 0.4 %
receiving myelosuppressive therapy : 0.4 %
patients receiving myelosuppressive : 0.4 %
therapy anticipated outcome : 0.4 %
anticipated outcome cure : 0.4 %
been reported patients : 0.4 %
controlled clinical trials : 0.4 %
indicated patients receiving : 0.4 %
not indicated patients : 0.4 %
effects clinical trials : 0.4 %
cardiovascular events stroke : 0.4 %
events stroke administered : 0.4 %
greater risks death : 0.4 %
experienced greater risks : 0.4 %
concomitant myelosuppressive chemotherapy : 0.4 %
clinical studies patients : 0.4 %
stroke administered erythropoiesis-stimulating : 0.4 %
red blood cell : 0.4 %
Chronic Renal Failure : 0.4 %
anemia due concomitant : 0.4 %
Aranesp indicated treatment : 0.4 %
Failure rsaquo visit : 0.4 %
indicated treatment anemia : 0.4 %
completion chemotherapy course : 0.2 %
chemotherapy course Aranesp : 0.2 %
over weeks contribute : 0.2 %
following completion chemotherapy : 0.2 %
weeks contribute risks : 0.2 %
cure Discontinue following : 0.2 %
ESAs not indicated : 0.2 %
outcome cure Discontinue : 0.2 %
course Aranesp contraindicated : 0.2 %
Discontinue following completion : 0.2 %
rise g dL : 0.2 %
access thrombosis rate : 0.2 %
vascular access thrombosis : 0.2 %
Aranesp contraindicated patients : 0.2 %
thrombosis rate hemoglobin : 0.2 %
rate hemoglobin rise : 0.2 %
g dL over : 0.2 %
contribute risks Cases : 0.2 %
hemoglobin rise g : 0.2 %
dL over weeks : 0.2 %
Cases pure red : 0.2 %
antibodies erythropoietin have : 0.2 %
neutralizing antibodies erythropoietin : 0.2 %
associated neutralizing antibodies : 0.2 %
cytopenias associated neutralizing : 0.2 %
erythropoietin have been : 0.2 %
have been reported : 0.2 %
patients treated Aranesp : 0.2 %
reported patients treated : 0.2 %
chemotherapy ESAs not : 0.2 %
other cytopenias associated : 0.2 %
without other cytopenias : 0.2 %
cell aplasia PRCA : 0.2 %
red cell aplasia : 0.2 %
pure red cell : 0.2 %
contraindicated patients uncontrolled : 0.2 %
aplasia PRCA severe : 0.2 %
PRCA severe anemia : 0.2 %
or without other : 0.2 %
anemia or without : 0.2 %
severe anemia or : 0.2 %
risks Cases pure : 0.2 %
uncontrolled hypertension Patients : 0.2 %
increased risks death : 0.2 %
ESAs increased risks : 0.2 %
other ESAs increased : 0.2 %
response ESA therapy : 0.2 %
cardiovascular events controlled : 0.2 %
events controlled clinical : 0.2 %
cancer events included : 0.2 %
patients cancer events : 0.2 %
trials patients cancer : 0.2 %
hemoglobin response ESA : 0.2 %
patients Aranesp other : 0.2 %
other patients Aranesp : 0.2 %
therapy be even : 0.2 %
be even greater : 0.2 %
even greater risk : 0.2 %
greater risk cardiovascular : 0.2 %
cardiovascular events mortality : 0.2 %
events mortality than : 0.2 %
ESA therapy be : 0.2 %
than other patients : 0.2 %
mortality than other : 0.2 %
events included myocardial : 0.2 %
treated Aranesp has : 0.2 %
clinical studies experienced : 0.2 %
studies experienced greater : 0.2 %
dL above Patients : 0.2 %
above Patients CRF : 0.2 %
participating clinical studies : 0.2 %
CRF participating clinical : 0.2 %
risk cardiovascular events : 0.2 %
hypertension Patients chronic : 0.2 %
Patients chronic renal : 0.2 %
failure CRF participating : 0.2 %
Patients CRF insufficient : 0.2 %
CRF insufficient hemoglobin : 0.2 %
stroke congestive heart : 0.2 %
infarction stroke congestive : 0.2 %
myocardial infarction stroke : 0.2 %
included myocardial infarction : 0.2 %
congestive heart failure : 0.2 %
heart failure hemodialysis : 0.2 %
insufficient hemoglobin response : 0.2 %
hemodialysis vascular access : 0.2 %
failure hemodialysis vascular : 0.2 %
patients uncontrolled hypertension : 0.2 %
administration PRCA has : 0.2 %
clinical trials most : 0.2 %
trials most commonly : 0.2 %
Aranesp clinical trials : 0.2 %
participating Aranesp clinical : 0.2 %
CRF participating Aranesp : 0.2 %
trials patients CRF : 0.2 %
patients CRF were : 0.2 %
hypertension hypotension muscle : 0.2 %
hypotension muscle spasm : 0.2 %
infection hypertension hypotension : 0.2 %
were infection hypertension : 0.2 %
CRF were infection : 0.2 %
patients CRF participating : 0.2 %
occurred patients CRF : 0.2 %
be switched other : 0.2 %
switched other ESAs : 0.2 %
not be switched : 0.2 %
should not be : 0.2 %
Patients should not : 0.2 %
other ESAs as : 0.2 %
ESAs as antibodies : 0.2 %
Seizures have occurred : 0.2 %
have occurred patients : 0.2 %
cross-react Seizures have : 0.2 %
antibodies cross-react Seizures : 0.2 %
as antibodies cross-react : 0.2 %
muscle spasm most : 0.2 %
spasm most commonly : 0.2 %
com Site Map : 0.2 %
Site Map Amgen : 0.2 %
Chemotherapy com Site : 0.2 %
com Chemotherapy com : 0.2 %
Amgen com Chemotherapy : 0.2 %
Map Amgen All : 0.2 %
Amgen All rights : 0.2 %
site use US : 0.2 %
use US only : 0.2 %
reserved site use : 0.2 %
rights reserved site : 0.2 %
All rights reserved : 0.2 %
dyspnea Amgen com : 0.2 %
fever dyspnea Amgen : 0.2 %
concomitant chemotherapy were : 0.2 %
chemotherapy were fatigue : 0.2 %
due concomitant chemotherapy : 0.2 %
patients anemia due : 0.2 %
trials patients anemia : 0.2 %
were fatigue edema : 0.2 %
fatigue edema nausea : 0.2 %
diarrhea fever dyspnea : 0.2 %
vomiting diarrhea fever : 0.2 %
nausea vomiting diarrhea : 0.2 %
edema nausea vomiting : 0.2 %
anemia Patients should : 0.2 %
antibody-mediated anemia Patients : 0.2 %
receiving ESAs while : 0.2 %
ESAs while undergoing : 0.2 %
patients receiving ESAs : 0.2 %
reported patients receiving : 0.2 %
also been reported : 0.2 %
while undergoing treatment : 0.2 %
undergoing treatment hepatitis : 0.2 %
interferon ribavirin sudden : 0.2 %
ribavirin sudden loss : 0.2 %



sm
Total: 243
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