Efficacy and safety of reslizumab in severe asthma patients with inadequate response to omalizumab: a multicentre, open-label, pilot studydoi:10.1016/j.jaip.2019.01.017Luis Perez de LlanoBorja CosioChristian DomingoLuis Prieto Andres
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The purpose of this study was to examine the efficacy and safety of vitamin supplements with resveratrol (Resvega, Thea Laboratories) in patients with diabetic macular edema (DME). Methods Participants in this prospective, pilot study were 23 patients with DME, who were previously treated with ...
The purpose of this study was to examine the efficacy and safety of vitamin supplements with resveratrol (Resvega, Thea Laboratories) in patients with diabetic macular edema (DME). Methods Participants in this prospective, pilot study were 23 patients with DME, who were previously treated with ...
Real-world safety of treatment with mepolizumab and reslizumab in patients with severe eosinophilic asthmadoi:10.1016/j.jaci.2018.12.301Ordóñez Pinilla, Karen A.Camacho, Beatriz MoyaRodríguez, Consuelo FernandezFernandez Crespo, Jesus F.
SAFETY DEVICE AGAINST RECURRENCE RISKS FOR RESAIRCH EQUIPMENT.CRISTINI, BRUNO TULLIOCRISTINI BRUNO TULLIO
This analysis evaluated efficacy and safety of BAY 94-9027, an extended-half-life recombinant factor VIII (FVIII), in the surgical setting. Patients participating in an open-label BAY 94-9027 clinical trial who underwent major surgery were included in the analysis. Investigator/surgeon assessment ...
Safety and efficacy of ambulatory management of secondary spontaneous pneumothorax: A case seriespneumothoraxprimary spontaneous pneumothoraxspontaneous pneumothoraxpleural catheterpleural diseasesambulatory caresecondary spontaneous pneumothoraxIntroduction The optimal management of pneumothorax remains undefined. There is...
Buildings' outer environment is significant for some kinds of crime. Spatial blind areas are adverse to crime prevention and control which is a key issue of the defense safety design. A favorable buildings' outer environment(abbr: BOE) provides an entertainment and communication place for residents...
The objective was to characterize the safety profile of revefenacin 88μg and 175μg over 52 weeks of treatment. In this randomized, parallel-group, 52-week trial (NCT02518139), 1055 participants with moderate to very severe COPD received revefenacin 88μg or 175μg in a double-blind ...