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The safety assessment of ustekinumab on psoriasis and psoriatic arthritis: A real-world analysis based on the FDA adverse event reporting system database.
タグ:
FAERS
2025/2/24
Endocrine Adverse Reactions of Tyrosine Kinase Inhibitors in Combination With Immune Checkpoint Inhibitors.
タグ:
FAERS
2025/2/23
Risk of acute renal failure associated with combined use of SGLT2 inhibitors and potentially nephrotoxic drugs: an epidemiological surveillance study based on the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2025/2/22
A comprehensive exploration of adverse reactions to lapatinib: a disproportionate analysis based on the FAERS database.
タグ:
FAERS
2025/2/22
A disproportionality analysis of surgical site infections across multiple sclerosis disease modifying therapies.
タグ:
FAERS
2025/2/22
Safety profiles of sevoflurane in pediatric patients: a real-world pharmacovigilance assessment based on the FAERS database.
タグ:
FAERS
2025/2/25
Update of safety profile of levonorgestrel: a disproportionality analysis based on FAERS from 2004 to 2023.
タグ:
FAERS
2025/2/25
A pharmacovigilance study based on the FAERS database focusing on anticoagulant and hormonal drugs that induce vaginal hemorrhage.
タグ:
FAERS
2025/2/25
Real-world study of medication-related osteonecrosis of the jaw from 2010 to 2023 based on Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2025/2/24
Investigating Drug-Induced Thyroid Dysfunction Adverse Events Associated With Non-Selective RET Multi-Kinase Inhibitors: A Pharmacovigilance Analysis Utilizing FDA Adverse Event Reporting System Data.
タグ:
FAERS
2025/2/24
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