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View Information Collection (IC)
View Information Collection (IC)
IC Title:
[NCEZID] Multistate investigation of serious adverse events, including deaths, of unknown etiology following ceftriaxone administration_Sep 2024-Present
Agency IC Tracking Number:
0920-1011-25-0015
IC Status:
New
Obligation to Respond:
Voluntary
CFR Citation:
Information Collection Instruments:
Document Type
Form No.
Form Name
Instrument File
URL
Available Electronically?
Can Be Submitted Electronically?
Electronic Capability
Form and Instruction
0920-1011
Case Report Form - Ceftriaxone Injection in Healthcare Settings - Public Health Departments
CDC Case Report Form - Serious Adverse Events Following Ceftriaxone Injection - PRA.pdf
N/A
No
Fillable Fileable
Form and Instruction
0920-1011
Case Report Form - Ceftriaxone Injection in Healthcare Settings - Healthcare Providers
CDC Case Report Form - Serious Adverse Events Following Ceftriaxone Injection - PRA.pdf
N/A
No
Fillable Fileable
Federal Enterprise Architecture Business Reference Module
Line of Business:
Disaster Management
Subfunction:
Emergency Response
Privacy Act System of Records
Title:
09-20-0113 - Epidemic Investigation Case Records
FR Citation:
51 FR 42466
Number of Respondents:
60
Number of Respondents for Small Entity:
0
Affected Public:
Individuals or Households
Percentage of Respondents Reporting Electronically:
0 %
Approved
Program Change Due to New Statute
Program Change Due to Agency Discretion
Change Due to Adjustment in Agency Estimate
Change Due to Potential Violation of the PRA
Previously Approved
Annual Number of Responses for this IC
90
0
90
0
0
0
Annual IC Time Burden (Hours)
45
0
45
0
0
0
Annual IC Cost Burden (Dollars)
0
0
0
0
0
0
Documents for IC
Title
Document
Date Uploaded
0920-1011 EEI GenIC Request Memo
GenIC Request Form for Emergency Epidemic Investigation_Serious adverse events 24-25(2)_02132025(2).docx
02/14/2025
Letter of Support - CSTE
letter of support for CDC to coordinate multi-state adverse events investigation.pdf
02/14/2025
Burden Request Memo
Burden Memo_serious adverse events24-25_02132025(2).docx
02/14/2025
Non-Research Determination
Non-research determination_Serioius Adverse Events Following Cefriaxone Injection.pdf
02/14/2025
Email Request for Approval - Acting Director_NCEZID Director
Eamil Emergency-Multistate_Ceftriaxone_Acting Director-NCEZID Director.msg
02/14/2025
Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.