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1 clusive; or indicates either serious risk or inefficacy.
2 hree dimensions of exhaustion, cynicism, and inefficacy.
4 most common reasons for discontinuation were inefficacy (30%), gastrointestinal symptoms (29%), medic
6 tion of all ISDs owing to clinical efficacy, inefficacy, adverse drug reaction (ADR), and other medic
7 s pathway after discontinuing phase 1 due to inefficacy; all other patients received another second-g
8 atients stopped taking the first drug due to inefficacy and 1,023 stopped the first drug due to toxic
10 rican Americans, whereas perceived treatment inefficacy and lacking trust in physicians were associat
13 n low drug accumulation at the tumor region (inefficacy) and drug-induced severe side effects (toxici
14 nt recommendations by authors, study-defined inefficacies, cognitive and depressive symptoms, discont
15 59 (10.6%) patients; only three events (drug inefficacy, gastritis, and reflux esophagitis) in two pa
16 d rate of second drug discontinuation due to inefficacy (hazard ratio [HR] 2.7, 95% confidence interv
21 were high (41-59%) and were more common for inefficacy in the placebo patients (71.4%), whereas they
22 nued their previous antipsychotic because of inefficacy (N=184), olanzapine was more effective than q
25 s substantial ATP equivalents, and (iii) the inefficacy of azole drugs against P. carinii can be expl
28 instay of arrhythmia treatment; however, the inefficacy of drug treatment and the potential that anti
30 nexpected practical consequences such as the inefficacy of many MHC class II tetramers in detecting s
33 o treatment, dropouts for any reason and for inefficacy of treatment, and important adverse events.
34 atment, study dropout for any reason and for inefficacy of treatment, use of drugs to treat parkinson
36 o patient withdrew from the study because of inefficacy or an adverse event related to pramipexole.
37 scontinued their assigned treatment owing to inefficacy or intolerable side effects or for other reas
39 In drug therapy, we face the problems of inefficacy or nonspecific effects; hence, nanosystems ar
41 rosis factor (anti-TNF) agent, due to either inefficacy or toxicity, are frequently switched to a sec
43 from criss-cross experiments, the functional inefficacy was not rooted in NOD Tregs, which suppressed
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