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Adverse event profiles of PCSK9 inhibitors alirocumab and evolocumab: Data mining of the FDA adverse event reporting system.
タグ:
FAERS
2022/7/13
Toxicity spectrum of immunotherapy in advanced lung cancer: A safety analysis from clinical trials and a pharmacovigilance system.
タグ:
FAERS
2022/7/12
Ocrelizumab-related neutropenia: Effects of age, sex and bodyweight using the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2022/7/11
Alopecia in Multiple Sclerosis Patients Treated with Disease Modifying Therapies.
タグ:
FAERS
2022/7/1
Detecting Drug-Drug Interactions in COVID-19 Patients.
タグ:
FAERS
2022/6/9
Antibacterial-associated acute kidney injury among older adults: A post-marketing surveillance study using the FDA adverse events reporting system.
タグ:
FAERS
2022/6/8
Association Between Antiosteoporotic Drugs and Risk of Acute Kidney Injury: A Cross-Sectional Study Using Disproportional Analysis and a Pharmacovigilance Database.
タグ:
FAERS
MDV
2022/6/7
Analysis of Adverse Reactions of Aspirin in Prophylaxis Medication Based on FAERS Database.
タグ:
FAERS
2022/6/7
Immune-related adverse events in older adults: Data mining of the FDA Adverse Event Reporting System.
タグ:
FAERS
2022/6/7
Comparability of clinical trials and spontaneous reporting data regarding COVID-19 vaccine safety.
タグ:
FAERS
VAERS
2022/6/30
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