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Post-marketing surveillance of AVIGAN tablets 200mg (SFTS)

Recruiting
Conditions
Severe Fever with Thrombocytopenia Syndrome
Registration Number
jRCT2031240539
Lead Sponsor
FUJIFILM Toyama Chemical Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
340
Inclusion Criteria

All patients treated with AVIGAN tablets 200 mg

Exclusion Criteria

none

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
-

Incidence of adverse drug reactions

Incidence of serious adverse events

Secondary Outcome Measures
NameTimeMethod
Mortality rate (by patient demographics and disease characteristics)at the time of discontinuation of AVIGAN tablets 200 mg or discharge (including death), cumulative mortality rate up to Day 28 after the start of administration

Mortality rate categorized by patient demographics and disease characteristics

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