Vaccine Adverse Event Reporting System Symptoms 2017

$179 / year

The signs, symptoms, and diagnoses provided are assigned codes and affixed to the case for indexing purposes that are found in this dataset. Information obtained from the original VAERS (Vaccine Adverse Event Reporting System) report, follow-up inquiries, and coding activities are stored in a secure computerized database for analysis. Scanned facsimiles of the original reports are also maintained in a computerized image-base for FDA and CDC vaccine surveillance activities.

Complexity

The Vaccine Adverse Event Reporting System (VAERS) was created by the Food and Drug Administration (FDA) and Centers for Disease Control and Prevention (CDC) to receive reports about adverse events that may be associated with vaccines. No prescription drug or biological product, such as a vaccine, is completely free from side effects. Vaccines protect many people from dangerous illnesses, but vaccines, like drugs, can cause side effects, a small percentage of which may be serious. VAERS is used to continually monitor reports to determine whether any vaccine or vaccine lot has a higher than expected rate of events.

Date Created

2017

Last Modified

2017-10-01

Version

2017-10-01

Update Frequency

Annual

Temporal Coverage

2017

Spatial Coverage

United States

Source

John Snow Labs; Department of Health and Human Services;

Source License URL

Source License Requirements

N/A

Source Citation

N/A

Keywords

Vaccine Adverse Event Reporting System Symptoms VAERS Data, VAERS Symptoms Data, VAERS Symptoms Data 2017, Vaccination Reporting System Symptoms 2017, VAERS Data 2017, Vaccination Symptoms Reporting System 2017, FDA Vaccine Symptom Reports, CDC Vaccine Reports, Vaccine Side Effects

Other Titles

VAERS Symptoms Report 2017, Vaccine Adverse Events and Symptoms 2017, Vaccine Adverse Event Reporting System Symptoms 2017

NameDescriptionTypeConstraints
VAERS_Identification_NumberUnique Vaccine Adverse Event Reporting System Identification Numberintegerlevel : Nominal
Symptom_Description1Adverse Event MedDRA (Medical Dictionary for Regulatory Activities) Term 1string-
Symptom_Version1_CodeMedDRA dictionary version number 1 pertaining to codes assigned to the symptomsnumberlevel : Nominal
Symptom_Description2Adverse Event MedDRA Term 2string-
Symptom_Version2_CodeMedDRA dictionary version number 2 pertaining to codes assigned to the symptomsnumberlevel : Nominal
Symptom_Description3Adverse Event MedDRA Term 3string-
Symptom_Version3_CodeMedDRA dictionary version number 3 pertaining to codes assigned to the symptomsnumberlevel : Nominal
Symptom_Description4Adverse Event MedDRA Term 4string-
Symptom_Version4_CodeMedDRA dictionary version number 4 pertaining to codes assigned to the symptomsnumberlevel : Nominal
Symptom_Description5Adverse Event MedDRA Term 5string-
Symptom_Version5_CodeMedDRA dictionary version number 5 pertaining to codes assigned to the symptomsnumberlevel : Nominal
VAERS_Identification_NumberSymptom_Description1Symptom_Version1_CodeSymptom_Description2Symptom_Version2_CodeSymptom_Description3Symptom_Version3_CodeSymptom_Description4Symptom_Version4_CodeSymptom_Description5Symptom_Version5_Code
684800Tic20
694876Tic20
701140Tic20
677382Pain20
677640Pain20
678551Rash20
679264Rash20
679794Rash20
680857Rash20
681670Rash20