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1 nappropriate for inclusion in a study (e.g., off-label use).
2  BDQ and DLM are extended beyond 24 weeks as off-label use.
3 riod of over 50 days is indicated in case of off-label use.
4  BDQ and DLM are extended beyond 24 weeks as off-label use.
5        Overall, 977 infants (18.8%) received off-label use.
6  treatment in the concept of repurposing and off-label use.
7 ved crizotinib therapy through an individual off-label use.
8 for Food and Drug Administration-approved or off-label use.
9 , with concomitant increases in dabigatran's off-label use.
10 e and duration of treatment as well as their off-label use.
11 among atypical antipsychotic medications for off-label use.
12 ere weakly associated with the likelihood of off-label use.
13  or headache, mood disorders, and unknown or off-label uses.
14 ontin, Pfizer, Inc., New York, New York) for off-label uses.
15 larly for P-tribe, despite being considered "off-label" use.
16 for Food and Drug Administration-approved or off-label use (0.74% vs 0.67%; p = 0.336; 33 vs 31 event
17 site end point was significantly higher with off-label use (adjusted hazard ratio [HR], 2.08; 95% con
18 s end point was not different at 1 year with off-label use (adjusted HR, 1.10; 95% CI, 0.79-1.54; P =
19 essel revascularization were associated with off-label use (adjusted HR, 1.49; 95% CI, 1.13-1.98; P =
20  reactions do not occur more frequently with off-label use, adverse drug reaction risk increases with
21            On-label use amounted to 70%, and off-label use amounted to 30%.
22 ce of adverse drug reactions associated with off-label use and evaluate off-label use as a risk facto
23                                    Excluding off-label use and pregnancy, 438 patients (78.6%) did no
24 ng and number of surfactant administrations, off-label use, and omission of use.
25 ard use, relative early safety is lower with off-label use, and the long-term effectiveness is lower
26                            However, it is an off-label use, and the potential side effects of dexmede
27 s associated with off-label use and evaluate off-label use as a risk factor for the development of ad
28 ibed promotion of the same drug for the same off-label use as was alleged by whistleblowers in the US
29 eterization laboratory-only eptifibatide (an off-label use) as procedural pharmacotherapy for patient
30 %), with hospitals in the highest tertile of off-label use associated with increased 30-day adverse c
31 re safe and efficacious in both on-label and off-label use but highlight differences between RCT and
32 rials in children, which might reduce unsafe off-label use by promoting more quickly proper labeling
33 agonists should not be offered routinely but off-label use can be considered in selected children.
34                                        Early off-label use data on TMVR in mitral valve-in-valve ther
35          Rate ratios were similar during the off-label use era and after pediatric labeling.
36 re not approved for use in the forehead, but off-label use for enhancement in this region is common.
37           EDTA chelation therapy has been in off-label use for the treatment of atherosclerosis.
38                   The CMS would pay only for off-label uses for which there is adequate evidence in i
39  seven ADRs lacking PI changes occurred with off-label use, for which PI change is not recommended by
40                                              Off-label use has been promoted because of the paucity o
41 is common in the ICU; however, the safety of off-label use has not been assessed.
42 ations, their unanticipated side effects and off-label use have contributed significantly to our unde
43  in Europe for olodaterol or indacaterol for off-label use in asthma or for pediatric use.
44 rol in clinical practice and to quantify the off-label use in asthma.
45 uring treatment for hypothyroidism or during off-label use in euthyroid individuals, has not proven t
46  disclosures made in articles related to the off-label use in question, determined the frequency of a
47 th BRAF inhibitors in clinical trials and as off-label use in routine practice by presenting 3 challe
48                                       Novel "off-label" uses in children for interleukin-1 receptor a
49                                     For each off-label use indication with 3 or more requests, random
50 ence on benefits for OS or PFS for requested off-label use indications.
51                                The extent of off-label use is a policy concern because the clinical b
52 tor medication in the United States, but its off-label use is associated with risks associated with t
53                Prior research indicates that off-label use is common in the ICU; however, the safety
54                                              Off-label use is composed of a roughly equal mix of chem
55 t in a health care system enabling access to off-label use, it was frequently intended as a first-lin
56  position) and articles (type, connection to off-label use, journal impact factor, citation count/yea
57 gle intravitreal injection of bevacizumab in off-label use (n = 33 eyes) or peripheral laser ablation
58                                              Off-label use occurred in 54.7% of all patients with bar
59            Caution is thus required with the off-label use of a perioperative intravenous n-3 PUFA em
60                                 In addition, off-label use of a third anti-VEGF agent, bevacizumab, a
61 ces (CMS) each created initiatives to reduce off-label use of antipsychotics in patients with dementi
62 MLV-related viruses, including XMRV, and the off-label use of antiretrovirals for the treatment of CF
63                  It could be argued that all off-label use of any agent should be deemed illegal.
64                      While investigating the off-label use of BDQ as salvage therapy, seven of 13 pat
65 d for the analysis of real-world data on the off-label use of bulevirtide in the setting of decompens
66 pares annulus measurements from 3D-TEE using off-label use of commercially available software with MD
67 eosinophilic esophagitis (EoE) is limited to off-label use of corticosteroids not optimized for esoph
68 eosinophilic esophagitis (EoE) is limited to off-label use of corticosteroids not optimized for esoph
69 yrin production, we treated the patient with off-label use of deferasirox to maintain iron deficiency
70 sting for drugs, and this policy perpetuates off-label use of devices and creates several issues in p
71                                 However, the off-label use of dexmedetomidine in premature infants ha
72                  Recent reports suggest that off-label use of drug-eluting stents is associated with
73                  Compared with on-label use, off-label use of drug-eluting stents is associated with
74 , highlighting the risks associated with the off-label use of drugs in newborn infants before safety
75  because of access to clinical trials and/or off-label use of drugs.
76                                              Off-label use of empagliflozin in 4 GSD-Ib patients with
77 he purpose of this study was to evaluate the off-label use of ePlex Blood Culture Identification Pane
78 D-19 are limited to supportive therapies and off-label use of FDA-approved drugs.
79 rend continued until the mid-1990s, when the off-label use of fenfluramine plus phentermine (fen-phen
80   Studies in the literature suggest that the off-label use of fibrin glue to close limbal conjunctiva
81 ed selective outcome reporting for trials of off-label use of gabapentin.
82 ugs and substantial medical need justify the off-label use of HCV PIs in select HIV/HCV-coinfected pe
83      Safety concerns arose because of common off-label use of higher doses, particularly after pediat
84 article, we review the existing data on this off-label use of LA CAB/RPV, discuss the motivations and
85    The results of small studies suggest that off-label use of low-dose oral minoxidil (LDOM) may be s
86     Current treatment strategies rely on the off-label use of medications for symptomatic treatment.
87                              We also discuss off-label use of medications studied for obesity and pro
88 ar use of nonsedating antihistamines and the off-label use of omalizumab.
89  the design of future prospective trials for off-label use of oncology drugs across four areas: trial
90                     For now, decisions about off-label use of recombinant factor VIIa remain at the p
91                           From 2000 to 2008, off-label use of rFVIIa in hospitals increased more than
92                                              Off-label use of rFVIIa in the hospital setting far exce
93 anti-mammarenavirus therapy is limited to an off-label use of ribavirin that has limited efficacy.
94 rent antiarenaviral therapy is limited to an off-label use of ribavirin that is only partially effect
95  antiarenaviral therapy being limited to the off-label use of ribavirin that is only partially effect
96 rent antiarenaviral therapy is limited to an off-label use of ribavirin that is only partially effect
97 anti-mammarenaviral therapy is limited to an off-label use of ribavirin whose efficacy is controversi
98 ile antiarenaviral therapy is limited to the off-label use of ribavirin, which is only partially effe
99 and antiarenaviral therapy is limited to the off-label use of ribavirin, which is only partially effe
100  mammarenavirus infections is limited to the off-label use of ribavirin, which is partially effective
101 w-potency antipsychotics (eg, quetiapine) or off-label use of sedative antihistamines (eg, promethazi
102 To evaluate patterns and adverse outcomes of off-label use of TAVR in US clinical practice.
103                                              Off-label use of TAVR.
104 ion, nonrandomized clinical experiences with off-label use of tenecteplase vs alteplase for AIS treat
105  resources to perform a validation study for off-label use of the breakpoints on their systems.
106 ts (n = 20) with baricitinib according to an off-label use of the drug.
107 art failure code was evaluated for potential off-label use of the drug.
108 t therapeutic intervention is limited to the off-label use of the wide-spectrum antiviral ribavirin.
109 fferent outcomes were observed following the off-label use of the Woven EndoBridge, or WEB, device fo
110 tream infections potentially attributable to off-label use of these water heaters to warm extracorpor
111                                          The off-label use of tirofiban might have affected our resul
112  To better assess the safety and efficacy of off-label use of Tpo-RAs during pregnancy, a multicenter
113 sis of these preliminary findings, temporary off-label use of Tpo-RAs for severe and/or refractory IT
114                                              Off-label use of transcatheter aortic and pulmonary valv
115 rm prophylactic treatment relies on lithium, off-label use of valproate, and growing use of modern an
116                                              Off-label use of vemurafenib (VMF) to treat BRAF(V600E)
117                                              Off-label use of VPA and other HDAC inhibitors for the t
118       Small-scale reports have evaluated the off-label use of WEB devices for the treatment of sidewa
119                              Trials were for off-label uses of gabapentin sponsored by Pfizer and Par
120 al companies have paid physicians to promote off-label uses of their products through a number of dif
121                                    Finally, "off-label" use of intravenous Ig has been evaluated for
122 rent antiarenaviral therapy is limited to an off-labeled use of the nucleoside analog ribavirin, whic
123                                Prevalence of off-label use ranged from 3.5% for both drugs to 12.4% f
124 cally appropriate cancer therapies including off-label uses recognized by established drug compendia
125         Among 3046 patients with cancer, 695 off-label use reimbursement requests in 303 different in
126 th Food and Drug Administration-approved and off-label use, respectively.
127 N-supported off-label indication, and 10% of off-label use was associated with an FDA-approved cancer
128                                    Potential off-label use was defined as no recorded diagnosis of ei
129                                              Off-label use was defined as use among adults with a rec
130                                              Off-label use was defined as use in restenotic lesions,
131               All other use was "off-label." Off-label use was divided by whether it conformed to Nat
132                                              Off-label use was intended as first-line treatment in 31
133 rventions were excluded, however, risk after off-label use was not significantly increased (P=0.23).
134 physician, and hospital characteristics with off-label use were explored with multivariable hierarchi
135 ependently associated with increased odds of off-label use, whereas diabetes mellitus, increasing age
136 and Drug Administration approval and 18 with off-label use with subjective benefit).
137           Delays in evaluation may result in off-label use without dosing information as the only acc

 
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