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Streamlining Considerations for Safety Measures: A Predictive Model for Addition of Clinically Significant Adverse Reactions to Japanese Drug Package Inserts.
タグ:
JADER
FAERS
2024/3/14
A real-world study of antifibrotic drugs-related adverse events based on the United States food and drug administration adverse event reporting system and VigiAccess databases.
タグ:
FAERS
2024/3/11
Reversible cerebral vasoconstriction syndrome and posterior reversible encephalopathy syndrome following vaccination: analysis of the VAERS database and systematic review.
タグ:
VAERS
FAERS
2024/3/11
Fibrosing colonopathy associated with cysteamine bitartrate delayed-release capsules in cystinosis patients.
タグ:
FAERS
2024/3/11
Safety monitoring of bivalent mRNA COVID-19 vaccine among pregnant persons in the vaccine adverse event reporting System – United States, September 1, 2022 – March 31, 2023.
タグ:
VAERS
FAERS
2024/3/11
Risk-stratified monitoring for sulfasalazine toxicity: prognostic model development and validation.
タグ:
CPRD
2024/3/8
VigiBase Pharmacovigilance Studies on Antidepressant-Related Adverse Reactions: A Scoping Review.
タグ:
VigiBase
2024/3/6
Adverse Events Following COVID-19 Vaccination in Adolescents: Insights From Pharmacovigilance Study of VigiBase.
タグ:
VigiBase
2024/3/6
A Reduction in the Number of Hospitalized Cases of Acute Meningitis during the COVID-19 Pandemic in Japan.
タグ:
DPC
2024/3/4
A nationwide epidemiological study of testicular torsion: Analysis of the Japanese National Database.
タグ:
NDB
2024/3/8
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