15 day report Form VAERS   30977-3

LOINC Code


LOINC code30977-3
name15 day report Form VAERS
descriptionThis term corresponds to item 26 in the Vaccine adverse event reporting system (VAERS) form. Serious, unexpected adverse experiences must be submitted to the FDA no later than 15 calendar days of initial receipt of the information by the applicant. Check yes if this report meets criteria specified in the biologic regulations for reports of serious and unexpected adverse events (21 CFR section 600.80).
statusACTIVE

Fully-Specified Name

component15 day report
propertyFind  =  Finding
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemForm
scaleOrd  =  Ordinal:  Ordered categorical responses, e.g., 1+, 2+, 3+; positive, negative; reactive, indeterminate, nonreactive.
methodVAERS

Additional Names

short name15 day report VAERS

Basic Attributes

classVACCIN
type2  Clinical
order vs. observationObservation

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

Member of these Panels

55140-8Vaccine Adverse Event Reporting System (VAERS) panel

History/Usage

first released
last updated2.42
last change typeMIN  - change to field other than name

Related Names

Finding
Findings
Ordinal
Point in time
QL
Qual
Qualitative
Random
Screen
VACCINE

Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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