Adverse Event Reporting System trang 1 tải miễn phí từ TAILIEUCHUNG

"Adverse Event Reporting System" trang 1 - tải miễn phí từ Tailieuchung

Adverse reaction profiles of hemorrhagic adverse reactions caused by direct oral anticoagulants analyzed using the Food and Drug Administration Adverse Event Reporting System (FAERS) database and the Japanese Adverse Drug Event Report (JADER) database

Adverse reaction profiles of hemorrhagic adverse reactions caused by direct oral anticoagulants analyzed using the Food and Drug Administration Adverse Event Reporting System (FAERS) database and the Japanese Adverse Drug Event Report (JADER) database

9 59 0

Evaluation of dabigatran and warfarin associated hemorrhagic events using the FDA adverse event reporting system database stratified by age

Evaluation of dabigatran and warfarin associated hemorrhagic events using the FDA adverse event reporting system database stratified by age

10 85 0

Torsades de pointes and QT prolongation associations with antibiotics: A pharmacovigilance study of the FDA adverse event reporting system

Torsades de pointes and QT prolongation associations with antibiotics: A pharmacovigilance study of the FDA adverse event reporting system

5 57 0

Báo cáo y học: "Adverse Event Profiles of Platinum Agents: Data Mining of the Public Version of the FDA Adverse Event Reporting System, AERS, and Reproducibility of Clinical Observations"

5 47 0

Antipsychotics associated serious adverse events in children: An analysis of the FAERS database

Antipsychotics associated serious adverse events in children: An analysis of the FAERS database

6 74 0

Identification and characteristics of time-related shifts in suicide-related event frequency during smoking cessation treatment with varenicline

Identification and characteristics of time-related shifts in suicide-related event frequency during smoking cessation treatment with varenicline

7 73 0

Rhabdomyolysis associations with antibiotics: A pharmacovigilance study of the FDA adverse event reporting system (FAERS)

Rhabdomyolysis associations with antibiotics: A pharmacovigilance study of the FDA adverse event reporting system (FAERS)

6 58 0

Clostridium difficile infection risk with important antibiotic classes: An analysis of the FDA adverse event reporting system

Clostridium difficile infection risk with important antibiotic classes: An analysis of the FDA adverse event reporting system

6 70 0

Perceived occurrence of an adverse event affects patient-reported outcomes after total hip replacement

Perceived occurrence of an adverse event affects patient-reported outcomes after total hip replacement

8 29 1

báo cáo khoa học:

báo cáo khoa học: "Hypersensitivity reactions to anticancer agents: Data mining of the public version of the FDA adverse event reporting system, AERS"

6 49 0

Báo cáo y học: "Platinum Agent-Induced Hypersensitivity Reactions: Data Mining of the Public Version of the FDA Adverse Event Reporting System, AER"

7 33 0

CFSAN Adverse Event Reporting System Voluntary and Mandatory Reports on 5-Hour Energy, Monster Energy, and Rockstar Energy Drink

CFSAN Adverse Event Reporting System Voluntary and Mandatory Reports on 5-Hour Energy, Monster Energy, and Rockstar Energy Drink

18 78 0

Surveillance for Safety After Immunization: Vaccine Adverse Event Reporting System (VAERS) — United States, 1991–2001

Surveillance for Safety After Immunization: Vaccine Adverse Event Reporting System (VAERS) — United States, 1991–2001

28 43 1

Guidance for Industry - How to Complete the Vaccine Adverse Event Reporting System Form (VAERS-1)

Guidance for Industry - How to Complete the Vaccine Adverse Event Reporting System Form (VAERS-1)

19 50 2

Large-scale combining signals from both biomedical literature and the FDA Adverse Event Reporting System (FAERS) to improve post-marketing drug safety signal detection

Large-scale combining signals from both biomedical literature and the FDA Adverse Event Reporting System (FAERS) to improve post-marketing drug safety signal detection

10 41 1

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