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Systematic analysis of safety profile for darunavir and its boosted agents using data mining in the FDA Adverse Event Reporting System database.
タグ:
FAERS
2021/6/16
Five Years of Sacubitril/Valsartan-a Safety Analysis of Randomized Clinical Trials and Real-World Pharmacovigilance.
タグ:
FAERS
EudraVigilance
VigiBase
2021/6/15
Anaphylactic risk related to omalizumab, benralizumab, reslizumab, mepolizumab, and dupilumab.
タグ:
FAERS
2021/6/15
Reporting of Thromboembolic Events with JAK Inhibitors: Analysis of the FAERS Database 2010-2019.
タグ:
FAERS
2021/6/14
Augmenting aer2vec: Enriching distributed representations of adverse event report data with orthographic and lexical information.
タグ:
FAERS
2021/6/11
Distributed Ledger Infrastructure to Verify Adverse Event Reporting (DeLIVER): Proposal for a Proof-of-Concept Study.
タグ:
FAERS
2021/6/11
Evaluation of rivaroxaban-, apixaban- and dabigatran-associated hemorrhagic events using the FDA-Adverse event reporting system (FAERS) database.
タグ:
FAERS
2021/6/11
Assessing Adverse Drug Reactions Reported for New Respiratory Medications in the FDA Adverse Event Reporting System Database.
タグ:
FAERS
2021/6/10
Age-Associated Changes in Adverse Events Arising From Anti-PD-(L)1 Therapy.
タグ:
FAERS
2021/6/1
Comparative pharmacovigilance assessment of mortality with pimavanserin in Parkinson disease-related psychosis.
タグ:
FAERS
2021/6/1
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