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1 e St-Cp group (63 versus 173; P<0.001), both serious (11 versus 46; P<0.001) and nonserious (52 versu
2                                Delirium is a serious acute neurocognitive condition frequently occurr
3 aced with such a wide variety of potentially serious adverse consequences, prescribers need to evalua
4  (GC)-induced ocular hypertension (OHT) is a serious adverse effect of prolonged GC therapy that can
5 hrough which clozapine may act to cause this serious adverse effect.
6  Like alcohol and tobacco, cannabis can have serious adverse effects on health, and some people have
7 placebo with mandatory dose escalation if no serious adverse effects were experienced.
8 t (29 [13%] of 223 vs 141 [64%] of 219) or a serious adverse event (11 [5%] of 223 vs 63 [29%] of 219
9  Incident decompensation was the most common serious adverse event (7% overall).
10                                          One serious adverse event (transient atrial fibrillation) oc
11                                          One serious adverse event during deferred treatment (interst
12                              The most common serious adverse event in the active surveillance group w
13 5%) and 22 (8%) patients had an on-treatment serious adverse event in the mepolizumab and placebo gro
14                              The most common serious adverse event in the vascular-targeted photodyna
15                                           No serious adverse event occurred in more than one particip
16 quartile range, 20-30 mo), no patients had a serious adverse event or relapse of vasculitis.
17 ety and regulatory affairs personnel to meet serious adverse event reporting requirements.
18 b and 54 (20%) of 265 assigned placebo had a serious adverse event that was judged by the investigato
19                                 At least one serious adverse event was reported in 65 (41%) of 157 pa
20  2.90, p = 0.6176; 1 death was reported as a serious adverse event).
21 l adhesions with obstruction as a severe and serious adverse event, which was considered as unrelated
22  arthropathy in one participant was the only serious adverse event.
23 lled studies reported low rates of death and serious adverse events (0% to 1.25%) in nontransported p
24                                           17 serious adverse events (3%) were reported during the stu
25  of 78 patients vs 81 [99%] of 82 patients), serious adverse events (36 [46%] vs 38 [46%]), and death
26                                   No deaths, serious adverse events (AEs), Grade 4 AEs or AEs leading
27 tients in the placebo group; the most common serious adverse events (affecting >/=2% of patients) wer
28  140 in the placebo group; the most frequent serious adverse events (affecting >/=2% of patients) wer
29 stive heart failure, or CVD death), and (ii) serious adverse events (hypotension, syncope, electrolyt
30 hose in the placebo group, or in the risk of serious adverse events (in 8.3% in the vaccine group and
31 endent factors associated with the number of serious adverse events (OR 3.07 [95% CI 1.75-5.38; p=0.0
32                                              Serious adverse events (regardless of relation to study
33 o significant difference in the incidence of serious adverse events (RR: 1.02; 95% CI: 0.94 to 1.09)
34 for IS contraindications were predefined and serious adverse events (SAEs) were reported to ethics co
35 tissue sarcoma group) had treatment-emergent serious adverse events (SAEs), five of whom had immune-r
36 re underpowered to identify risk factors for serious adverse events (SAEs), thereby limiting their in
37  days, and 3-, 6-, and 12-months for safety (serious adverse events [SAE]), and efficacy endpoints: e
38 nt difference between groups in the rates of serious adverse events and serious infections.
39  treatment costs, treatment-related risks of serious adverse events and subsequent costs, and quality
40                        Mortality and overall serious adverse events at 90 days were not significantly
41                                     No other serious adverse events attributable to angiotensin II we
42  loss in children and is not associated with serious adverse events attributed to its use.
43 nce of large differences in risk of systemic serious adverse events between these two anti-VEGF drugs
44                                  Overall and serious adverse events did not differ between the flecai
45                          The overall rate of serious adverse events did not differ between treatment
46 tic cancer, medullary thyroid carcinoma, and serious adverse events did not differ significantly betw
47                                              Serious adverse events for all patients included anastom
48 y outcome as percentage of participants with serious adverse events in all participants who were inje
49 d, were febrile neutropenia (27 [17%] of 155 serious adverse events in patients who received doxorubi
50 who received doxorubicin and 15 [12%] of 130 serious adverse events in patients who received gemcitab
51                           Treatment-emergent serious adverse events occurred in 103 (7%) women in the
52                                              Serious adverse events occurred in 11% of the patients w
53                                A total of 38 serious adverse events occurred in 15 patients (5 events
54                                              Serious adverse events occurred in 15% of the patients i
55                                              Serious adverse events occurred in 19 patients (33%) in
56                                              Serious adverse events occurred in 2 patients in the IFN
57                                 Drug-related serious adverse events occurred in 28 (38%) of 74 patien
58                                         Five serious adverse events occurred in 4 cases (15%), includ
59                                              Serious adverse events occurred in 75 (19%) patients in
60                                        Eight serious adverse events occurred in each group.
61                                        Three serious adverse events occurred that were unrelated to t
62                               Two unexpected serious adverse events occurred, both for the first pati
63 o episodes of serious hypoglycaemia or other serious adverse events occurred.
64                                              Serious adverse events occurring in 5% or more of patien
65                                              Serious adverse events occurring in more than 2% of pati
66                                              Serious adverse events occurring in more than two patien
67 lesterol and safety outcomes, either for all serious adverse events or any of the other nine prespeci
68                                There were no serious adverse events or discontinuations due to advers
69           There was no significant excess of serious adverse events prespecified as being of special
70 se events, representing 111 (39%) of all 285 serious adverse events recorded, were febrile neutropeni
71 30672 treatment for 14 days was safe with no serious adverse events reported.
72                                              Serious adverse events such as infection, urinary retent
73  and no placebo recipients experienced fatal serious adverse events suspected to be study drug-relate
74                              The most common serious adverse events that occurred through week 24 wer
75                              The most common serious adverse events were anaemia (eight [4%]), upper
76                   Overall adverse events and serious adverse events were balanced between the two gro
77                           No vaccine-related serious adverse events were documented.
78                                              Serious adverse events were experienced by 35 (18%) pati
79                                     Thirteen serious adverse events were identified among recipients
80                                              Serious adverse events were more frequent the in G-CSF a
81                                              Serious adverse events were rare (6 patients) and were o
82                                              Serious adverse events were recorded in three (3%) patie
83                                         Four serious adverse events were reported during the conduct
84                                        Eight serious adverse events were reported during the course o
85                                              Serious adverse events were reported in 102 (25%) of 403
86                                              Serious adverse events were reported in 13 (13%) of 103
87                            Treatment-related serious adverse events were reported in 133 (37%) patien
88                                              Serious adverse events were reported in 134 (23%) of 573
89                                              Serious adverse events were reported in 155 (49%) versus
90                                              Serious adverse events were reported in 20 (22%) patient
91                                              Serious adverse events were reported in 24% of the patie
92                                              Serious adverse events were reported in 56 (58%) eltromb
93                                              Serious adverse events were reported in 64 (22%) of 288
94                                           11 serious adverse events were reported in seven (25%) pati
95 0 (32%) of 156 in the placebo group, and 181 serious adverse events were reported in total, 95 (52%)
96                                        Three serious adverse events were reported, all in patients in
97 in severity, and no severe adverse events or serious adverse events were reported.
98                                           No serious adverse events were reported.
99                            Treatment-related serious adverse events were similar between groups (13 [
100                                              Serious adverse events within 12 months after injection
101 s are the incidence of study product-related serious adverse events within 180 days, grade 3 solicite
102 idences of blood-product use, infection, and serious adverse events, as well as 28-day mortality, did
103  Central Africa because of the occurrence of serious adverse events, including death, in persons with
104               Seven (44%) of 16 patients had serious adverse events, most of which were related to th
105              There were no treatment-related serious adverse events, no treatment-related unsolicited
106                         11 (8%) patients had serious adverse events, none of which were deemed relate
107 nuations occurred because of adverse events, serious adverse events, or deaths in patients who receiv
108                        The three most common serious adverse events, representing 111 (39%) of all 28
109                                        Three serious adverse events-febrile neutropenia, intestinal p
110 relapsed and 2 discontinued treatment due to serious adverse events.
111      Study drugs were well tolerated with no serious adverse events.
112 and fall (n=6; 20%); four patients (13%) had serious adverse events.
113 f-care identification of persons at risk for serious adverse events.
114 s required discontinuation of therapy due to serious adverse events.
115 ences in the risk of death, cancer, or other serious adverse events.
116 t strategy, however, could be an increase in serious adverse events.
117 and PD-1 were associated with lowest risk of serious adverse events.
118              16 (2%) of 664 participants had serious adverse events.
119 icipants who had lower versus higher ARIs in serious adverse events.
120                     Six (3%) patients had 11 serious adverse events: one (2%) patient in the placebo
121  30 days after surgery; delirium; mortality; serious adverse events; and neurocognition.
122                         12 patients reported serious adverse events; haemolysis and pyrexia were the
123                 Two (1%) of 166 patients had serious adverse events; neither were considered related
124  that hormone therapy use is associated with serious adverse health effects in postmenopausal women,
125            One unexpected, possibly related, serious adverse reaction that occurred 7 days after a 64
126                              The most common serious adverse reaction was infection occurring in five
127                                              Serious adverse reactions necessitating hospitalisation
128                                           No serious adverse reactions were recorded and other safety
129                                              Serious AEs (SAEs) occurred infrequently.
130                                              Serious AEs (SAEs) were recorded through 6 months postva
131   A novel weed has recently emerged, causing serious agronomic damage in one of the most important ma
132 ological forecasting, but here we consider a serious alternative based on collective human judgment.
133                                Epilepsy is a serious and common neurological disorder.
134                                 Obesity is a serious and growing worldwide health challenge.
135 luorescein angiography has shown potentially serious and long-term ocular effects that are present mo
136  12 months after the procedure, and rates of serious and minor adverse events within 30 days of the p
137                 Pulmonary embolism (PE) is a serious and prevalent cause of vascular disease.
138                              It is a common, serious, and often fatal condition among older patients.
139 here, along with open questions that require serious attention for full understanding of the molecula
140                          Pressure ulcers are serious, avoidable, costly and common adverse outcomes o
141  augment the host immune response to prevent serious bacterial infections, and represent a significan
142  to the data from such studies can result in serious bias in testing experimental effects.
143 d the OPN system play important roles in the serious bone abnormalities associated with MDD.
144                                              Serious brain disorders, such as the Alzheimer's Disease
145 welve participants (2.0%) were found to have serious cardiorespiratory conditions that had been previ
146 venous thrombosis (DVT) remains a common and serious cardiovascular problem with both fatal and long-
147 hile water erosion is identified as the most serious cause of soil degradation globally, global patte
148      The development of such platforms faces serious challenges at both the technological level due t
149 ate that plant cells can respond flexibly to serious challenges of compromised MT-dependent MT nuclea
150 ve a responsibility to rebut and decry these serious challenges to human health and scientific integr
151  catheters that block urine flow and lead to serious clinical complications.
152  healthy individuals and a central aspect of serious clinical conditions, such as eating disorders.
153 esorption by osteoclasts (OCs) can result in serious clinical outcomes, including bone loss that may
154 elderly, had poor prognostic factors, or had serious comorbidities.
155                   Stent thrombosis (ST) is a serious complication following coronary stenting.
156 ant lymphoproliferative disorder (PTLD) is a serious complication in organ transplant recipients and
157                Peritoneal fibrosis (PF) is a serious complication in various clinical settings, but t
158                               Infection is a serious complication of cardiovascular-implantable elect
159 UND & AIMS: Hepatic encephalopathy (HE) is a serious complication of cirrhosis and is associated with
160      Acute chest syndrome (ACS) is a common, serious complication of sickle cell disease (SCD) and a
161 nation, surgical site infections (SSI) are a serious complication that can result in delayed wound he
162 or persistent infections are correlated with serious complications in humans, understanding these pro
163 tions, there was a higher rate of predefined serious complications in the elderly group (5 events vs.
164                                         Most serious complications led to hospitalization, and most G
165                                  The risk of serious complications was higher in the elderly group.
166                                         Four serious complications were evaluated: posterior capsule
167                                           No serious complications were observed.
168                                There were no serious complications, such as lens subluxation or endop
169 es has lifesaving potential, but can lead to serious complications.
170 on and the lack of an approved vaccine raise serious concerns regarding preparedness to combat this e
171  quantify the global burden of this rare but serious condition.
172 s may offer another option for managing this serious condition.
173  sciences but light-induced side effects are serious confounding factors.
174 tworks extracted from the multiplex may have serious consequences in the characterization of the true
175                        Plant pathogens cause serious crop losses worldwide.
176  20% (11/55) of BHFS survivors suffer from a serious delay of >/=6 months.
177 nisitic bacteria that are capable of causing serious diseases, mainly in immunocompromised individual
178 as a result of increased recognition of this serious disorder but more so because of the increased us
179                   Anorexia nervosa (AN) is a serious eating disorder characterized by self-starvation
180  to most immersed solid surfaces, leading to serious economic and ecological consequences for the mar
181                                              Serious encephalopathy occurred in 3 patients (11%); 2 c
182 ed (FI)-RSV vaccine has been associated with serious enhanced respiratory disease (ERD).
183  a reliable passivating layer to survive the serious environmental corrosion during handling and cycl
184 , an organophosphate insecticide, has raised serious environmental health concerns since it is a pote
185 ess Phosphorus (P) in agriculture is causing serious environmental problems like eutrophication of la
186 haze events often occurred in China, causing serious environmental problems.
187 IVIg group) and 4 in the open IVIg phase had serious events.
188 did not cause irreversible loss of vision or serious eye damage.
189  item from each domain, the 10-point SaFETy (Serious fighting, Friend weapon carrying, community Envi
190 n enterohemorrhagic bacteria responsible for serious foodborne outbreaks that causes diarrhoea, fever
191  resistant bacterial pathogens have become a serious global human health threat, and conjugative plas
192 ity from fisheries is clearly among the most serious global threats for marine ecosystems, affecting
193 er clinical development for the treatment of serious Gram-negative infections.
194 ne seems to be associated with a low rate of serious harms, but no study evaluated risks of transport
195                               Influenza is a serious hazard to human health that causes hundreds of t
196 us (HCV)-mediated chronic liver disease is a serious health problem around the world and often causes
197  bladder outlet obstruction continue to be a serious health problem.
198  contaminated vegetables and grains may pose serious health risks.
199 rages, and packaging, with the potential for serious health, as well as significant economic and soci
200 h levels of exposure, indicate a potentially serious human health burden from air pollution in the Ka
201                   Staphylococcus aureus is a serious human pathogen with remarkable adaptive powers.
202                               No episodes of serious hypoglycaemia or other serious adverse events oc
203               Ebola virus disease (EVD) is a serious illness with mortality rates of 20-90% in variou
204 improve the quality of life of children with serious illnesses and their families.
205              Non-human-derived PAbs can have serious immunoreactivity complications, and when "humani
206                    The projected losses have serious implications for the hydropower, municipal and a
207 before neurological disease becomes overt or serious.IMPORTANCE The detection of highly compartmental
208 outpatient visits, and diagnoses were rarely serious in the ambulatory setting but potentially life t
209               Burkholderia species can cause serious infection in CF and themselves affect key oxidas
210    We found no evidence of increased odds of serious infection in comparisons of the different treatm
211                                              Serious infection occurred in 1.3% of the patients treat
212                                  The risk of serious infection should not be a key discriminator for
213                A total of 283 patients had a serious infection; the incidence rates with 95% confiden
214                      We assessed the risk of serious infections for biologics used to treat psoriasis
215  is an opportunistic pathogen that can cause serious infections in immunocompromised individuals.
216                           SSIs, particularly serious infections resulting in hospitalization or surgi
217                                   Three (2%) serious infections, all in patients in the ixekizumab ev
218 rsus without risk factors for development of serious infections, such as contact lens wearers (P = 0.
219 s in the rates of serious adverse events and serious infections.
220 s are available to treat patients with these serious infections.
221 d Beetle (ALB) Anoplophora glabripennis is a serious invasive forest pest in several countries includ
222 ctional, elastic SEIs that overcome the most serious limitations of spontaneously formed interphases
223         However, these platforms suffer from serious limitations, including small sample sizes.
224 s drugs, acyclovir and its derivatives, have serious limitations, such as low bioavailability and sev
225             However, democratic methods have serious limitations.
226 n women (heterogeneity P<0.001), but RRs for serious liver complications appeared higher in women (he
227 ae and is the single most important cause of serious lower respiratory tract infections in young chil
228        Glomerulonephritis is one of the most serious manifestations of systemic lupus erythematous (S
229 maternal mortality worldwide and may lead to serious maternal complications, including stroke, eclamp
230 geneous genomic population and may result in serious medical conditions.
231 es modern society, contributing to a host of serious medical problems.
232 ticipants were 359 diverse probationers with serious mental health problems and functional impairment
233 to improve quality of care for patients with serious mental illness and cardiovascular risk factors.
234 st as a site for therapeutic intervention in serious mental illness, yet we know very little about th
235  abstinence in outpatients with co-occurring serious mental illnesses.
236 e 2 diabetes(T2D) are the most prevalent and serious metabolic diseases affecting people worldwide.
237  2014, rates of death prior to discharge and serious morbidities decreased among the NICUs in this st
238 ted that approximately 100,000 people suffer serious morbidity and 10,000 people die each year from t
239       No significant difference was found in serious morbidity between HSHs and LSHs for bariatric or
240               Main outcome measures included serious morbidity, in-hospital mortality, intensive care
241 se in the incidence of a diverse spectrum of serious neurologic syndromes.
242  in the brain tissue of HIV patients without serious neurological disease is consistent with their em
243 due to its association with microcephaly and serious neurological disorders.
244 ts in the once daily group (one of which was serious; none led to treatment discontinuation) and 68 (
245 ensive arm, but there were no differences in serious nonhematological toxicities.
246 events were mild to moderate in severity; no serious ocular adverse events were reported.
247     Post-transplant tuberculosis (PTTB) is a serious opportunistic infection in renal graft recipient
248                               Drugs treating serious or life-threatening conditions can receive US Fo
249 time to any adverse event (primary outcome); serious or nonserious events; partial and complete remis
250  there were no differences between groups in serious or other adverse events.
251 cal or mild disease, infection can result in serious outcomes, including acute respiratory distress s
252 is full of small migrant insects, among them serious pests (e.g. some species of aphid), but also man
253 oxic or antimicrobial agents for controlling serious plant pathogens.
254                     Delirium is a common and serious postoperative complication.
255  genome data analysis to the cloud can raise serious privacy concerns.
256 ological contamination of nanomaterials is a serious problem hampering their widespread use in biomed
257                                    Given the serious problem of drug resistance and the adverse side
258                                 A common and serious problem with this therapy is the patient's immun
259                                              Serious problems in the experimental design and data int
260     There were no pericardial effusions, but serious procedure/device-related events occurred in 3 pa
261                     Delirium is a common and serious psychiatric syndrome caused by an underlying med
262 ics and occasional pandemics, representing a serious public health concern.
263 volving illicit and prescription drugs are a serious public health issue.
264            Traumatic brain injury (TBI) is a serious public health problem, often with devastating co
265  Cancer is currently one of the world's most serious public health problems.
266 pollution, including black carbon, entails a serious public health risk because of its carcinogenic p
267 nem-resistant Enterobacteriaceae (CRE) are a serious public health threat.
268 t our overall approach of nanomedicine needs serious reevaluation.
269 elusive how leukemic cells could acquire the serious resistance against RUNX1-inhibition therapies an
270  is the causative agent of whooping cough, a serious respiratory infection causing hundreds of thousa
271 ge indicated that the predictive ability for serious respiratory morbidity increased from 34 weeks (A
272 , and 23% were other race/ethnicity), 88 had serious respiratory morbidity, 257 infants had neurosens
273                                              Serious respiratory morbidity, neurosensory impairment a
274 stability of photoelectrode materials impose serious restrictions on its advancement.
275   The quality of evidence is very low due to serious risk of bias and imprecision.
276 ed bleeding and pathological thrombosis pose serious risks to hospitalized patients.
277 n emerging pathogen causally associated with serious sequelae in fetuses, inducing fetal microcephaly
278 e Unit (ICU) patients and is associated with serious short- and long-term consequences, including re-
279                    This article examines the serious shortcomings that characterize the current taxon
280                                     The most serious side effects were exacerbation of left ventricul
281 ic cleft lip with palate (NSCLP) is the most serious sub-phenotype of non-syndromic orofacial clefts
282 s due to the rapid industrialization poses a serious threat on the environment.
283 he extraction of tantalum and niobium pose a serious threat to human beings and the environment due t
284 ection by HRP2-based RDTs, would represent a serious threat to malaria elimination efforts.
285 g, acidification, and deoxygenation, poses a serious threat to marine organisms.
286 phere, from Africa via Asia, it has become a serious threat to pregnant women, causing microcephaly a
287  outbreak of Zika virus (ZIKV) has imposed a serious threat to public health.
288 borne pathogen Campylobacter is considered a serious threat to public health.
289 nly driving species to extinction, they pose serious threats to human health and wellbeing.
290 iruses cause inclusion body disease (IBD), a serious transmissible disease of snakes.
291 ide and 43 (10%) taking carbamazepine-CR had serious treatment-emergent adverse events, and 47 (11%)
292               36 (10%) of 370 patients had a serious treatment-related adverse event.
293               Six (11%) of 53 patients had a serious treatment-related adverse event: autoimmune diso
294  in the twice daily group (two of which were serious; two led to treatment discontinuation).
295  of gemfibrozil in warfarin users results in serious underanticoagulation.
296  children who develop this complication have serious underlying medical disorders.
297 s of current oncology clinical practice have serious, unmet health information technology needs.
298 was associated with greater adjusted odds of serious ventricular arrhythmias (OR, 31.8; 95% CI, 4.3-2
299 disorder that is progressive and may lead to serious visual impairment.
300 timicrobial-resistant (AMR) bacteria poses a serious worldwide health concern.

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