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Ingenol Mebutate Is Associated With Increased Reporting Odds for Squamous Cell Carcinoma in Actinic Keratosis Patients, a Pharmacovigilance Study of the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2022/12/11
Hepatitis B Virus Reactivation in Cancer Patients Undergoing Immune Checkpoint Inhibitors Therapy: A Systematic Review.
タグ:
FAERS
2022/12/10
Consolidated Overview of Notifiable Adverse Events in the U.S. President’s Emergency Plan for AIDS Relief’s Voluntary Medical Male Circumcision Program Through 2020.
タグ:
FAERS
2022/11/9
Linezolid and the risk of QT interval prolongation: A pharmacovigilance study of the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2022/11/9
Real-world study of antiresorptive-related osteonecrosis of jaw based on the US food and drug administration adverse event reporting system database.
タグ:
FAERS
2022/11/8
Gastrointestinal adverse events associated with semaglutide: A pharmacovigilance study based on FDA adverse event reporting system.
タグ:
FAERS
2022/11/8
Skin cancer signal associated with phosphodiesterase inhibitors: gaining insight through the FDA pharmacovigilance database.
タグ:
FAERS
2022/11/6
[Elucidation of Pathology in Urological Diseases and Creation of New Therapeutics].
タグ:
FAERS
2022/11/4
Trends in copper versus hormonal intrauterine device breakage reporting within the United States’ Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2022/11/4
Safety Monitoring of Bivalent COVID-19 mRNA Vaccine Booster Doses Among Persons Aged >/=12 Years – United States, August 31-October 23, 2022.
タグ:
FAERS
VAERS
2022/11/4
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