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A Standardized Dataset of a Spontaneous Adverse Event Reporting System.
タグ:
FAERS
2022/3/26
Topical ophthalmic beta-blockers are associated with ocular pseudopemphigoid: A pharmacovigilance study of antiglaucoma medications utilising the FDA adverse event reporting system.
タグ:
FAERS
2022/3/23
Dropped head syndrome: a rare adverse drug reaction identified in the FDA adverse event reporting system and review of case reports in the literature.
タグ:
FAERS
2022/3/23
Updated Insights on Cardiac and Vascular Risks of Proton Pump Inhibitors: A Real-World Pharmacovigilance Study.
タグ:
FAERS
2022/3/15
Adverse drug reactions of montelukast and pranlukast: Analysis of the Korea database.
タグ:
FAERS
KAERS
2022/3/13
Pulmonary tuberculosis associated with immune checkpoint inhibitors: a pharmacovigilance study.
タグ:
FAERS
2022/3/13
Safety of mRNA vaccines administered during the initial 6 months of the US COVID-19 vaccination programme: an observational study of reports to the Vaccine Adverse Event Reporting System and v-safe.
タグ:
FAERS
VAERS
2022/3/11
Sodium-Glucose Cotransporter 2 Inhibitor Use Associated With Fournier’s Gangrene: A Review of Case Reports and Spontaneous Post-Marketing Cases.
タグ:
FAERS
2022/3/1
Transient Lymphocytic Colitis After SARS-CoV2 mRNA Vaccine.
タグ:
FAERS
VAERS
2022/2/8
Cutaneous Toxicity Associated With Enfortumab Vedotin: A Real-Word Study Leveraging U.S. Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2022/2/8
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