<p>AE, adverse event; DLT, dose-limiting toxicity (DLTs were defined as grade ≥3 infusion-related neurologic AEs and nonhematologic AEs not responsive to symptom-directed therapy); PR, probably related; PS, possibly related; NR, not related; TEAE, treatment-emergent adverse event.</p><p>Summary of dose-limiting toxicities and serious adverse events.</p
When a novel additional adverse effect is reported for a marketed medicine, the medical information ...
When a novel additional adverse effect is reported for a marketed medicine, the medical information ...
Introduction: Traditional dose-limiting toxicity (DLT) definition, which uses grade (G) 3-4 toxicity...
<p>Serious adverse events in patients who completed all pharmacokinetic assessments (N = 25) and in ...
<p>Abbreviations: A/E (adverse effects), TCZ (tocilizumab), IFX (infliximab), ETN (etanercept), ADA ...
<p><b>Abbreviations:</b> TEAEs = treatment-emergent-adverse-events;NCI-CTC = National Cancer Institu...
<p>Only adverse events recorded in 3 patients or more have been listed in this table. A total of 196...
<p>AE, adverse event; SAE, serious adverse event; NA, not applicable.</p><p>Summary of safety outcom...
Summary of Safety by age group and dose cohorts and most common treatment-related adverse events by ...
a<p>Clinicians judged whether the adverse events recorded in the medical diaries of the patients wer...
*<p>A treatment-emergent adverse event was defined as an adverse event that was reported on or after...
The Adverse Outcome Pathway (AOP) framework provides a template that facilitates understanding of co...
When a novel additional adverse effect is reported for a marketed medicine, the medical information ...
The Adverse Outcome Pathway (AOP) framework provides a template that facilitates understanding of co...
The Adverse Outcome Pathway (AOP) framework provides a template that facilitates understanding of co...
When a novel additional adverse effect is reported for a marketed medicine, the medical information ...
When a novel additional adverse effect is reported for a marketed medicine, the medical information ...
Introduction: Traditional dose-limiting toxicity (DLT) definition, which uses grade (G) 3-4 toxicity...
<p>Serious adverse events in patients who completed all pharmacokinetic assessments (N = 25) and in ...
<p>Abbreviations: A/E (adverse effects), TCZ (tocilizumab), IFX (infliximab), ETN (etanercept), ADA ...
<p><b>Abbreviations:</b> TEAEs = treatment-emergent-adverse-events;NCI-CTC = National Cancer Institu...
<p>Only adverse events recorded in 3 patients or more have been listed in this table. A total of 196...
<p>AE, adverse event; SAE, serious adverse event; NA, not applicable.</p><p>Summary of safety outcom...
Summary of Safety by age group and dose cohorts and most common treatment-related adverse events by ...
a<p>Clinicians judged whether the adverse events recorded in the medical diaries of the patients wer...
*<p>A treatment-emergent adverse event was defined as an adverse event that was reported on or after...
The Adverse Outcome Pathway (AOP) framework provides a template that facilitates understanding of co...
When a novel additional adverse effect is reported for a marketed medicine, the medical information ...
The Adverse Outcome Pathway (AOP) framework provides a template that facilitates understanding of co...
The Adverse Outcome Pathway (AOP) framework provides a template that facilitates understanding of co...
When a novel additional adverse effect is reported for a marketed medicine, the medical information ...
When a novel additional adverse effect is reported for a marketed medicine, the medical information ...
Introduction: Traditional dose-limiting toxicity (DLT) definition, which uses grade (G) 3-4 toxicity...