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Nursing home leaders’ perception of factors influencing the reporting of elder abuse and neglect: a qualitative study.
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FAERS
2020/8/8
Incidence of venous and arterial thromboembolic events reported in the tofacitinib rheumatoid arthritis, psoriasis and psoriatic arthritis development programmes and from real-world data.
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FAERS
2020/8/8
Adverse Events Reported to the United States Food and Drug Administration Related to Caffeine-Containing Products.
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2020/8/6
Ocular Adverse Events Induced by Immune Checkpoint Inhibitors: A Comprehensive Pharmacovigilance Analysis.
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2020/8/5
Liver Injury with Ulipristal Acetate: Exploring the Underlying Pharmacological Basis.
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2020/8/5
Post-Marketing Safety Concerns with Esketamine: A Disproportionality Analysis of Spontaneous Reports Submitted to the FDA Adverse Event Reporting System.
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FAERS
2020/8/28
Safety concerns reported by consumers, manufacturers and healthcare professionals: A detailed evaluation of opioid-related adverse drug reactions in the FDA database over 15 years.
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2020/8/28
Angioedema with sacubitril/valsartan: Trial-level meta-analysis of over 14,000 patients and real-world evidence to date.
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FAERS
2020/8/26
Clinical Research Informatics.
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2020/8/22
Adverse event profile differences between rituximab and ocrelizumab: Findings from the FDA Adverse Event Reporting Database.
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FAERS
2020/8/22
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