論文・技術情報追加のお知らせ

Clostridium difficile Infection Risk with Important Antibiotic Classes: An Analysis of the FDA Adverse Event Reporting System.

抗生物質使用によるクロストリジウム・ディフィシル感染リスク評価研究

対象DB：FAERS

Fluoxetine and Risk of Bleeding in Patients Aged 60 Years and Older Using the Korea Adverse Event Reporting System Database: A Case/Noncase Study.

フルオキセチンと出血のリスク症例/非症例研究

対象DB：KOREA　AERS

Adverse Drug Reactions Related to Mood and Emotion in Pediatric Patients Treated for Attention Deficit/Hyperactivity Disorder: A Comparative Analysis of the US Food and Drug Administration Adverse Event Reporting System Database.

ADHD小児患者における気分・感情に関連した有害薬物反応調査研究

対象DB：FAERS

Adverse events following purified chick embryo cell rabies vaccine in the Vaccine Adverse Event Reporting System (VAERS) in the United States, 2006-2016.

ニワトリ胚細胞のワクチンを対象とした有害事象研究

対象DB：VAERS

Myopathy with DPP-4 inhibitors and statins in the real world: investigating the likelihood of drug-drug interactions through the FDA adverse event reporting system.

DPP-4阻害剤とスタチンによるミオパチーとの薬物相互作用に関する調査研究

対象DB：FAERS

Interaction between paracetamol and lamotrigine: new insights from the FDA Adverse Event Reporting System (FAERS) database.

パラセタモールとラモトリジンの相互作用に関する研究

対象DB：FAERS

Antibiotic treatment and flares of rheumatoid arthritis: a self-controlled case series study analysis using CPRD GOLD.

関節リウマチ患者における抗生物質の使用とフレアの発生との関連性調査研究

対象DB：CPRD

Genome-wide association study of statin-induced myopathy in patients recruited using the UK clinical practice research datalink.

スタチン誘発性ミオパチーの遺伝的リスク因子調査研究

対象DB：CPRD