Hepatitis B Virus Reactivation Associated With Direct-Acting Antiviral Therapy for Chronic Hepatitis C Virus: A Review of Cases Reported to the U.S. Food and Drug Administration Adverse Event Reporting System

Susan J. Bersoff-Matcha; Kelly Cao; Mihaela Jason; Adebola Ajao; S. Christopher Jones; Tamra Meyer; Allen Brinker

doi:10.7326/m17-0377

Hepatitis B Virus Reactivation Associated With Direct-Acting Antiviral Therapy for Chronic Hepatitis C Virus: A Review of Cases Reported to the U.S. Food and Drug Administration Adverse Event Reporting System

Annals of Internal Medicine ◽

10.7326/m17-0377 ◽

2017 ◽

Vol 166 (11) ◽

pp. 792 ◽

Cited By ~ 93

Author(s):

Susan J. Bersoff-Matcha ◽

Kelly Cao ◽

Mihaela Jason ◽

Adebola Ajao ◽

S. Christopher Jones ◽

...

Keyword(s):

Reporting System ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Virus Reactivation ◽

Event Reporting ◽

Direct Acting Antiviral ◽

B Virus ◽

Chronic Hepatitis C Virus ◽

Direct Acting ◽

The U.S

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Comment on: “Safety of Marketed Cancer Supportive Care Biosimilars in the U.S.: A Disproportionality Analysis Using the Food and Drug Administration Adverse Event Reporting System (FAERS) Database”

BioDrugs ◽

10.1007/s40259-021-00476-9 ◽

2021 ◽

Author(s):

Joerg Putzke ◽

Scott Haughie ◽

Kelly H. Zou ◽

Gopinath M. Ranganna

Keyword(s):

Adverse Event ◽

Supportive Care ◽

Drug Administration ◽

Reporting System ◽

Food And Drug Administration ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Disproportionality Analysis ◽

Event Reporting ◽

The U.S

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Adverse events reported to the U.S. Food and Drug Administration Adverse Event Reporting System for tisagenlecleucel

American Journal of Hematology ◽

10.1002/ajh.26246 ◽

2021 ◽

Author(s):

Graça M. Dores ◽

Christopher Jason ◽

Manette T. Niu ◽

Silvia Perez‐Vilar

Keyword(s):

Adverse Event ◽

Adverse Events ◽

Drug Administration ◽

Reporting System ◽

Food And Drug Administration ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Event Reporting ◽

The U.S

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Hypoglycemia Associated with Direct Acting Anti‐hepatitis C Virus Drugs: an Epidemiologic Surveillance Study of the FDA Adverse Event Reporting System (FAERS)

Clinical Endocrinology ◽

10.1111/cen.14660 ◽

2021 ◽

Author(s):

Yu Zhou ◽

Wenhuo Xie ◽

Chenhua Zheng ◽

Libin Liu ◽

Zhou Chen ◽

...

Keyword(s):

Adverse Event ◽

Hepatitis C Virus ◽

Hepatitis C ◽

Reporting System ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Surveillance Study ◽

Event Reporting ◽

Epidemiologic Surveillance ◽

Direct Acting

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Empirical estimation of under-reporting in the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS)

Expert Opinion on Drug Safety ◽

10.1080/14740338.2017.1323867 ◽

2017 ◽

Vol 16 (7) ◽

pp. 761-767 ◽

Cited By ~ 27

Author(s):

Yasser M. Alatawi ◽

Richard A. Hansen

Keyword(s):

Adverse Event ◽

Drug Administration ◽

Reporting System ◽

Food And Drug Administration ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Empirical Estimation ◽

Event Reporting ◽

The U.S

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Injection-Site Nodules Associated With the Use of Exenatide Extended-Release Reported to the U.S. Food and Drug Administration Adverse Event Reporting System

Diabetes Spectrum ◽

10.2337/diaspect.28.4.283 ◽

2015 ◽

Vol 28 (4) ◽

pp. 283-288 ◽

Cited By ~ 6

Author(s):

S. C. Jones ◽

D. L. Ryan ◽

V. S. W. Pratt ◽

A. Niak ◽

A. D. Brinker

Keyword(s):

Adverse Event ◽

Injection Site ◽

Drug Administration ◽

Extended Release ◽

Reporting System ◽

Food And Drug Administration ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Event Reporting ◽

The U.S

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Comparison of brand versus generic antiepileptic drug adverse event reporting rates in the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS)

Epilepsy Research ◽

10.1016/j.eplepsyres.2017.06.007 ◽

2017 ◽

Vol 135 ◽

pp. 71-78 ◽

Cited By ~ 11

Author(s):

Md. Motiur Rahman ◽

Yasser Alatawi ◽

Ning Cheng ◽

Jingjing Qian ◽

Annya V. Plotkina ◽

...

Keyword(s):

Adverse Event ◽

Antiepileptic Drug ◽

Drug Administration ◽

Reporting System ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Event Reporting ◽

Drug Adverse Event ◽

Reporting Rates ◽

The U.S

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