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1 s were mostly mild or moderate and none were serious.
2 res careful matching of blood types to avoid serious adverse consequences.
3                           No vaccine-related serious adverse effects were found in the dose-ranging s
4 6 [1 = difficult, 5 = easy]) and was without serious adverse effects.
5 4%) in the control group reported at least 1 serious adverse event (adjusted RR, 1.72 [95% CI, 0.7 to
6 rse events (OR 2.65, 95% CI: 1.04-6.80), any serious adverse event (OR 2.30, 95% CI: 1.18-4.48), seri
7                                          One serious adverse event (SAE) that resulted in death was p
8                                   At least 1 serious adverse event developed in 12 patients (24%) in
9 Peri-prosthetic joint infections (PJI) are a serious adverse event following joint replacement surger
10 icipants randomised to rosuvastatin, and one serious adverse event in each group.
11                       Pneumonia was the only serious adverse event in more than 2% of patients (seven
12                 One 3-year-old patient had a serious adverse event of accidental ribavirin overdose r
13                                              Serious adverse event rates could not be determined with
14 l outcome data at week 16-17, or sooner if a serious adverse event requiring knowledge of the study d
15               At least one treatment-related serious adverse event was reported in 25 (10%) patients
16      25 (42%) patients reported at least one serious adverse event, which most commonly was an infect
17  was well tolerated, with a low incidence of serious adverse events (16%).
18 43.9% [43/98] vs 25.5% [25/98]; P = .01) and serious adverse events (27.6% [27/98] vs 12.2% [12/98];
19         Few participants in either group had serious adverse events (3 [2.4%] vs. 5 [4.0%]).
20                                              Serious adverse events (AEs) occurred in 10% of imipenem
21                                           No serious adverse events (AEs) related to treatment were r
22 PVR) is associated with a risk of procedural serious adverse events (SAE) and exposure to ionizing ra
23                The total incidence of AE and serious adverse events (SAE) was calculated.
24    Within clinical trials, rates of systemic serious adverse events (SAEs) after anti-VEGF treatment
25 ment outcomes, culture-conversion rates, and serious adverse events (SAEs) during treatment.
26 nth 36 in part 1, and symptomatic dengue and serious adverse events (SAEs) up to Month 36 in both par
27     Endpoints were solicited/unsolicited and serious adverse events (SAEs), biochemical/hematological
28 te the existing evidence for serious and non-serious adverse events after ivermectin exposure in preg
29 amounts, reduce time to recovery, and reduce serious adverse events among hospitalized patients not r
30 years in the placebo group; the incidence of serious adverse events and adverse events leading to wit
31 sivir probably improves recovery and reduces serious adverse events and may reduce mortality and time
32                   There were no drug-related serious adverse events and no treatment-related deaths.
33                                           No serious adverse events attributed to ruxolitinib were ob
34 7 mothers in the dolutegravir group reported serious adverse events compared with 14 (11%) of 131 in
35 ssociated with an increased risk of death or serious adverse events compared with allopurinol.
36 30%) in the placebo group (with 6 infectious serious adverse events developing among 4 patients [9%])
37 te nomograms to calculate the probability of serious adverse events during OFC for individual patient
38 tment-emergent adverse events, including six serious adverse events in five patients and 13 discontin
39                                              Serious adverse events in the lower-threshold group incl
40                                              Serious adverse events included 1 suicide attempt, relat
41                        The outcomes of these serious adverse events included 16 deaths, 4 of which we
42  regimen was safe, with no treatment-related serious adverse events observed.
43                                   No related serious adverse events occurred during the second year.
44                                        Three serious adverse events occurred during the study (pulmon
45                                              Serious adverse events occurred equally between groups.
46                                              Serious adverse events occurred in 10% of participants o
47                                              Serious adverse events occurred in 115 (34%) patients in
48                                     Nonfatal serious adverse events occurred in 12/72 (16.7%) in the
49                                              Serious adverse events occurred in 22.7% and 21.7%, resp
50                            Treatment-related serious adverse events occurred in 25 (24%) patients and
51                                              Serious adverse events occurred in 250 (45%) of 559 pati
52                                              Serious adverse events occurred in 33 (10%) of 332 patie
53                                              Serious adverse events occurred in 7.2% of patients in t
54                                       All 14 serious adverse events occurred in patients who received
55                            Treatment-related serious adverse events occurred in seven (12%) patients
56                            Treatment-related serious adverse events occurred in six (14%) of 42 patie
57                                        Three serious adverse events occurred in the biomechanical foo
58                      No intervention-related serious adverse events occurred, and few adverse effects
59                         Four non-DBS-related serious adverse events occurred, including one suicide a
60 %) in the rituximab group (with 9 infectious serious adverse events occurring among 6 patients [12%])
61                           No vaccine-related serious adverse events or severe dengue virus disease we
62  adverse event (OR 2.30, 95% CI: 1.18-4.48), serious adverse events related to abnormal liver functio
63 not differ significantly between the groups; serious adverse events related to rhythm-control therapy
64 gs and are associated with increased risk of serious adverse events such as infusion reactions and an
65                                    Of the 16 serious adverse events unrelated to the study drugs, 4 (
66                                              Serious adverse events up to week 24 occurred in no pati
67  CI 232.71-243.57) per 100 patient-years and serious adverse events was 12.63 (95% CI 11.41-13.94) pe
68                             The incidence of serious adverse events was low and was similar in the va
69 p difference in the incidence or severity of serious adverse events was reported during the follow-up
70                                The number of serious adverse events was similar in both groups and un
71                             The frequency of serious adverse events was similar in the two groups.
72                                              Serious adverse events were assessed in all women who re
73                                           No serious adverse events were attributed to dihydroartemis
74 3.94) per 100 patient-years; the most common serious adverse events were infections at 4.13 (95% CI 3
75                              The most common serious adverse events were lower respiratory tract infe
76                           Adverse events and serious adverse events were minimal, but 2 deaths (7.4%)
77                                              Serious adverse events were more common with systematic
78                                              Serious adverse events were observed in ten (28%) patien
79                              The most common serious adverse events were pyrexia (n=9), pneumonia (n=
80                                              Serious adverse events were recorded in 30 and 40 patien
81                                           No serious adverse events were related to vaccination.
82                                          Two serious adverse events were reported - both resolved wit
83                                              Serious adverse events were reported for 18 (20%) of 90
84                                              Serious adverse events were reported for 18 (8%) patient
85                                    Any-cause serious adverse events were reported in 121 (45%) patien
86                                              Serious adverse events were reported in 4 (3%), 5 (3%),
87                                              Serious adverse events were reported in 84 of 182 patien
88                                              Serious adverse events were reported in five (3%) of 156
89                                        Eight serious adverse events were reported with capsular relea
90                                              Serious adverse events were similar between groups (112
91                                              Serious adverse events were similar in both groups (vita
92                          Cumulative rates of serious adverse events were similar in TAK-003 (4.0%) an
93 tinence, daily cigarette consumption change, serious adverse events, adverse events, dropouts due to
94 dose, including solicited adverse events and serious adverse events, and immunogenicity (seroprotecti
95 rare, with generally no group differences in serious adverse events, any adverse events, hospitalizat
96 rimary safety outcome (a composite of death, serious adverse events, or clinical grade 3 or 4 adverse
97                        36 individuals had 63 serious adverse events, which included 25 suicide attemp
98 c drugs on cardiac contractility can lead to serious adverse events.
99 All subjects completed the study without any serious adverse events.
100 s limited, it indicated no increased risk of serious adverse events.
101 sion at week 12 but was associated with more serious adverse events.
102 lement for MPOD volume and SC levels without serious adverse events.
103 ences of malaria, vaso-occlusive crises, and serious adverse events.
104 lar numbers of donor-specific antibodies and serious adverse events.
105 and safety, as measured by the occurrence of serious adverse events.
106           There were no intervention-related serious adverse events.
107  no significant between-group differences in serious adverse events.
108 erventional management, with a lower risk of serious adverse events.
109 ere no clinically relevant treatment-related serious adverse events.
110 rly after two of the four patients developed serious adverse events.
111 , and 5 (3.3%) vs 9 (6.1%) experienced other serious adverse events.
112  acute and chronic exposure to OPs can cause serious adverse health effects.
113  participants in the PRESERVE (Prevention of Serious Adverse Outcomes Following Angiography) trial wi
114 erize the relative risk for and incidence of serious adverse outcomes following the development of CA
115                                           17 serious adverse reactions occurred in 11 patients, and t
116  than with placebo (40.1% vs. 16.8%), but no serious adverse reactions were reported.
117 mes included cumulative incidence rates for (serious) adverse events.
118 ssociated with an increased relative risk of serious, adverse 90-day outcomes, the incidence of clini
119           The evidence for dupilumab-related serious AE is uncertain.
120                                              Serious AEs (n = 20; 48%) included infections (n = 14) a
121                Further, there were no ocular serious AEs (SAEs) and no cases of endophthalmitis.
122 Treatment was well tolerated in most however serious AEs can occur in those with advanced liver disea
123                                There were no serious AEs in any of the study arms.
124 nd polyneuropathy (n = 2); treatment-related serious AEs included 2 grade 3 polyneuropathies and 1 gr
125                               Two additional serious AEs were reported (rhinitis [JNJ-8678]; pneumoni
126 systemic events (SEs), adverse events (AEs), serious AEs, newly diagnosed chronic medical conditions,
127                                There were no serious AEs.
128                 Three (1.2%) patients had 12 serious AEs; most were cardiac disorders; all were unrel
129                 Retinal detachment (RD) is a serious and common condition, but genetic studies to dat
130 , and the associated health consequences are serious and costly.
131 en the groups was shown in the occurrence of serious and drug-related adverse events.
132                           The therapy led to serious and life-threatening toxic effects that were con
133  aimed to evaluate the existing evidence for serious and non-serious adverse events after ivermectin
134 egions as well as asymptomatic infections, a serious barrier to eliminating this disease.
135 ithout compromising hemostasis, thus causing serious bleeding and increased morbidity and mortality.
136 mbosis in humanized mice, but neither causes serious bleeding, establishing a causal link between par
137  primary outcome of death, disabling stroke, serious bleeding, or cardiac arrest.
138 nd derived structure distortion would induce serious capacity loss and voltage decay, further hinderi
139                        Strategies to prevent serious cardiac complications in this high-risk cohort o
140 bjectives were to determine the incidence of serious cardiac events (SCEs) in pregnant women with hea
141 d compared the rates of the composite of all serious cardiovascular events (MI, stroke, coronary reva
142 edian of 3.7 years of follow-up, 3,417 total serious cardiovascular events occurred in 2,003 individu
143       Canakinumab reduced the rates of total serious cardiovascular events, with rates per 100 person
144 s trialled in COVID-19 are unlikely to cause serious cardiovascular toxicity.
145 coronaviruses are not yet approved, posing a serious challenge to current global efforts aimed at con
146 tion of such complex forms of big data poses serious challenges to users of MD.
147  metastasis and resistance to therapy remain serious clinical challenges.
148 terpretative value and that there is often a serious collinearity issue for the gene-level models whi
149 s had an estimate 28-68% increased odds of a serious complication and a 58-60% increased odds of 30-d
150         Cytomegalovirus (CMV) infection is a serious complication in immunosuppressed patients, speci
151 nusoidal obstruction syndrome (VOD/SOS) is a serious complication post allogeneic hematopoietic stem
152 es, acute kidney injury (AKI) is a frequent, serious complication ranging from 10% to 30%.
153 th the lowest risk- and reliability-adjusted serious complication rates for each operation.
154 r discriminating any complication, 0.523 for serious complication, and 0.559 for readmission.
155  must be assessed on all radiographs because serious complications can arise if catheters are malposi
156                                              Serious complications requiring reoperation or producing
157                                           No serious complications such as blindness, anaphylactic re
158 tension, diabetes mellitus, and obesity, and serious complications such as stroke and heart failure.
159                                              Serious complications were predominantly cardiac and ass
160                                              Serious complications were significantly associated with
161 likely has no effect on severe desaturation, serious complications, apneic time, oxygenation, ICU len
162 sumption of contaminated crops is becoming a serious concern for human health.
163          Gut bacteria-associated sepsis is a serious concern in patients with gastrointestinal acute
164  is an infrequent but morbid and potentially serious condition associated with antiresorptive and ant
165  formation accounts for the etiology of many serious conditions including myocardial infarction, stro
166 ther, these findings highlight a potentially serious confound in prior work, raising new theoretical
167   Increasing air pollution in South Asia has serious consequences for air quality and human/ecosystem
168 his work establishes organic polaritons as a serious contender to the well-established GaAs platform
169 sing levels of antimicrobial resistance pose serious dangers to patients, population health, food sec
170 ndently associated with death or persistent, serious deterioration of health-related quality of life
171 improve the quality of life of children with serious disease and increase support for their parents a
172 ich is the causative agent of melioidosis, a serious disease that occurs in the tropics, and a potent
173 olating selected vibrational modes, leads to serious drawbacks for interrogation of the trapped phono
174                 Ground deformation can cause serious environmental issues such as infrastructure dama
175                    Anthraquinone dyes pose a serious environmental problem as their reinforced struct
176 ics and the access to cheap oil, is creating serious environmental problems.
177                Resident physicians made more serious errors during the intervention schedules than du
178 es that eliminated extended shifts made more serious errors than resident physicians assigned to sche
179                                The number of serious errors unitwide were likewise higher during the
180  Severe acute malnutrition (SAM) is the most serious form of undernutrition, characterized by wasting
181 g tool to tackle antimicrobial resistance, a serious global health problem.
182        SARS-CoV-2 infection has emerged as a serious global pandemic.
183 -related outcomes, with little to no risk of serious harm.
184                       Influenza B virus is a serious health concern for children, in particular, yet
185 olyfluoroalkyl substances (PFAS), which pose serious health concerns.
186                        Many individuals with serious health problems were experiencing significant pa
187                                          The serious health problems, recent healthcare experiences,
188             Eating raw oysters can come with serious health risks, as oysters can potentially contain
189 e and liver are associated with a variety of serious health risks.
190 les associated with death and/or persistent, serious health-related quality of life deterioration wer
191 otransporter 2 inhibitors reduce the risk of serious heart failure and adverse renal events, but the
192 ied in a patient with Tetralogy of Fallot, a serious heart valve defect, affects the substrate select
193         Major depressive disorder (MDD) is a serious, heterogeneous disorder accompanied by brain-rel
194   Inflammation is associated with a range of serious human conditions, including autoimmune and cardi
195 s central to the etiology of a wide range of serious human diseases, such as Alzheimer's disease and
196 ising advances to aid rural people to manage serious illness and to die in place.
197 n how to have meaningful conversations about serious illness using telecommunication.
198 k response was resource intensive and caused serious illness, particularly among unvaccinated childre
199 es that address the needs of all people with serious illness-related suffering and their caregivers.
200 ation of programs to alleviate the burden of serious illness-related suffering in these settings.
201 e proven benefits of nonhospice PC for other serious illnesses and cancer, there are no evidence-base
202 tic care at an early stage for patients with serious illnesses and their families is commonly referre
203 roperly evaluated as there can be underlying serious illnesses as in our patient.
204 teria, protozoa, and viruses, that can cause serious illnesses.
205 ion, this study demonstrates the potentially serious impact of introducing thinner, more flexible tis
206  visuospatial function domains were the most serious impaired domains in the major cognitive impairme
207 vior and are at a particularly high risk for serious impairment relative to others with these disorde
208                            Our findings have serious implications for the management of PCB contamina
209 e to false-positive dengue serology can have serious implications.
210 ls, principally in order to minimize risk of serious infection.
211      However, recent trends for IE and other serious infections among persons with substance use diso
212                 Rates of hospitalization for serious infections among persons with SUDs are increasin
213 Neutropenia and neutrophil dysfunction cause serious infections and inflammatory bowel disease in gly
214  is a gram-positive organism responsible for serious infections in humans, but as with many bacterial
215 on, and charges between hospitalizations for serious infections in patients with and without OUD.
216                In addition, the detection of serious infections may be more challenging owing to pati
217                                              Serious infections occurred in 2.5% and 1.8% of the pati
218  use disorder (OUD) who are hospitalized for serious infections requiring prolonged intravenous antib
219 oups had higher incidences of infections and serious infections vs placebo.
220 d no difference between groups in pneumonia, serious infections, any infection, hemorrhage, renal fai
221 rium of antifungals available to treat these serious infections.
222 tment may be feasible and safe for PWID with serious infections.
223 s; no guselkumab-treated patient died or had serious infections.
224  of 427 patients in the adalimumab group had serious infections.
225  group died from cardiac failure and two had serious infections; no guselkumab-treated patient died o
226 city score; sinusoidal obstruction syndrome; serious infections; WHO Bleeding Scale; transfusion requ
227 %) patients under active treatment developed serious infectious events, and two (10%) developed diver
228  virgifera (Coleoptera: Chrysomelidae), is a serious insect pest in the major corn growing areas of N
229 ed wing drosophila, Drosophila suzukii, is a serious invasive pest impacting the production of multip
230 g number of published articles can present a serious issue for both trainees and senior scientists al
231 l time-of-flight (TOF) MSI continues to be a serious issue.
232  by the SARS-CoV-2 has recently emerged as a serious jolt to human life and economy.
233 white-light emission properties, they pose a serious long-term environmental and health risk as they
234 y higher than use of systemic treatments for serious manifestations of the disease and diagnosis of l
235 ensure safety for patients being treated for serious methicillin-resistant Staphylococcus aureus infe
236                The overall rates of death or serious morbidity (DSM) and clinically-relevant fistula
237  be less effective than believed at reducing serious morbidity and mortality in this population, whic
238                                              Serious morbidity composite was significantly lower in p
239 ure to COVID-19 had increased probability of serious morbidity, healthcare seeking, hospitalization,
240                  Vancomycin is used to treat serious MRSA infections, but treatment failures occur de
241 ts management is a major challenge given the serious nature of the thrombotic disease observed, which
242  this particular experiment to highlight the serious need to consider the frame of reference of the e
243  synthetic polymeric materials that can pose serious negative environmental impacts, cellulose-based
244 of nanomaterials-based formulations to avoid serious neurotoxic complications, which may further lead
245 ug-resistant strains of this bacterium cause serious nosocomial infections and are the leading cause
246 priority" pathogen which is a major cause of serious nosocomial infections such as bacteremia, sepsis
247 quared) of 40 or higher or 35 or higher with serious obesity-related comorbidities.
248 ment, waste of administrative resources, and serious obstacles to wildlife protection.
249                                              Serious obstetric events were also examined.
250       Both SARS-CoV and MERS-CoV have caused serious outbreaks and epidemics in the past eighteen yea
251 ts aged >=65 years were admitted to Canadian Serious Outcomes Surveillance Network hospitals during t
252                  This silly sentence makes a serious point: As humans, we can flexibly generate and c
253 lable, some recent publications illustrate a serious potential failing in this domain: inclusion of r
254  sensitivity of these assays can represent a serious problem if the occurrence of experimental errors
255                            Malnutrition is a serious problem in the elderly while understanding flavo
256 fections after a craniotomy (SSI-CRAN) are a serious problem involving significant morbidity and cost
257                   This method suffers from a serious problem: The resulting ratios are highly correla
258                  OSCL and CL of gas are more serious problems due to the risk of long-term leakage fr
259                                              Serious procedure-related adverse events were uncommon.
260 stigating the relationship between sleep and serious psychological distress (SPD) have lacked racial/
261 hand exposure to e-cig aerosols has become a serious public health concern.
262 rticulate matter (PM) pollution has become a serious public health issue, especially with outbreaks o
263 eria is of critical importance in addressing serious public health problems.
264 emonstrate convincing evidence that BoV is a serious respiratory pathogen.
265 ly intake calculation, samples do not pose a serious risk to public health.
266 cause of congenital birth defects, and poses serious risks for immuno-compromised individuals.
267 nt concern in maize production, as they pose serious risks to human and animal health.
268                                 This poses a serious roadblock for clinical translation of this appro
269 sign was observational, 21 of 36 studies had serious ROB, and publication bias was possible.
270  However, use of CsA is associated with more serious side effects and worse clinical outcomes than FK
271  DEBs eliminates the need for stents so that serious side effects including in-stent restenosis and s
272 rials to treat metabolic syndrome due to the serious side effects such as hypertriglyceridemia and al
273 when initiated early in illness but can have serious side effects.
274 ration may improve outcomes in patients with serious streptococcal infections.
275    Enterococcus faecalis, long implicated in serious systemic infections and failure of root canal tr
276                             The frequency of serious TEAEs was similar between the groups (10% in the
277                                          All serious TEAEs were unrelated to treatment.
278                                    There are serious theoretical problems with the free-energy princi
279 ins, such as aflatoxin B(1) (AFB(1)), pose a serious threat as biological weapons due to their high t
280              These prime cases epitomize the serious threat that wildlife poisoning poses to biodiver
281 obally, and drug-resistant TB strains pose a serious threat to controlling the global TB epidemic.
282                Antimicrobial resistance is a serious threat to human health worldwide, prompting rese
283 I) is a devastating disease of poultry and a serious threat to public health.
284  viruses, are emerging pathogens that pose a serious threat to public health.
285           Such knowledge is needed to thwart serious threats to human health and calls to mind the pr
286                  Enterovirus 71 (EV71) poses serious threats to human health, particularly in Southea
287                                              Serious treatment-emergent adverse events in more than o
288                                              Serious treatment-emergent adverse events occurred in 93
289                              No drug-related serious treatment-emergent adverse events occurred.
290                                              Serious treatment-related adverse events occurred in 11
291                                              Serious treatment-related adverse events occurred in 30
292                              The most common serious treatment-related adverse events were nervous sy
293                                              Serious treatment-related adverse events were reported i
294                         14 (9%) patients had serious treatment-related adverse events, most commonly
295                        15 (11%) patients had serious treatment-related adverse events, the most commo
296                       Five (9%) patients had serious treatment-related adverse events.
297 re opportunistic infections in patients with serious underlying medical conditions, such as those wit
298 , and the ability of opioid drugs to produce serious undesired effects has been recognized for a simi
299 ar after vaccination with PCV20 or PCV13; no serious vaccine-related AEs were reported.
300 antaviruses are rodent-borne viruses causing serious zoonotic outbreaks worldwide for which no treatm

 
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