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A Real‑World Pharmacovigilance Study of FDA Adverse Event Reporting System (FAERS) for Mavacamten.
タグ:
FAERS
2024/8/21
Drug-induced erectile dysfunction: a real-world pharmacovigilance study using the FDA adverse event reporting system database.
タグ:
FAERS
2024/8/23
A real-world pharmacovigilance study of cardiac adverse events induced by sugammadex in the FDA adverse event reporting system.
タグ:
FAERS
2024/8/23
Are Alpha-2 Adrenergic Agonists Being Used in Infants?
タグ:
FAERS
2024/8/22
Indications and adverse events of teriparatide: based on FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/8/22
Association between antipsychotics and pulmonary embolism: a pharmacovigilance analysis.
タグ:
FAERS
2024/8/23
Systemic sclerosis and cancer in the UK: an epidemiological analysis using the clinical practice research datalink.
タグ:
CPRD
2024/8/13
Prevalence, risk factors and characterisation of individuals with long COVID using Electronic Health Records in over 1.5 million COVID cases in England.
タグ:
CPRD
2024/8/10
Impact of co-resident health and living alone on risk of hospital admission for people with Parkinson’s disease.
タグ:
CPRD
2024/8/10
Factors associated with long-term opioid use among patients with axial spondyloarthritis or psoriatic arthritis who initiate opioids.
タグ:
CPRD
2024/8/16
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