Others titles
- VAERS Database 2018
- Vaccine Adverse Events 2018
- Adverse Event Reporting System 2018
Keywords
- Adverse Event Reporting System Vaccine Information
- VAERS Vaccine Info Data
- VAERS Data 2018
- Vaccination Reporting System 2018
- Vaccine Adverse Event Reporting System VAERS Data
- VAERS Data
- FDA Vaccine Reports
- CDC Vaccine Reports
- Vaccine Side Effects
Vaccine Adverse Event Reporting System Vaccine Information 2018
A report to Vaccine Adverse Event Reporting System (VAERS) generally does not prove that the identified vaccine(s) caused the adverse event described. It only confirms that the reported event occurred sometime after the vaccine was given, which is what this dataset showcases. No proof that the event was caused by the vaccine is required in order for VAERS to accept the report. VAERS accepts all reports without judging whether the event was caused by the vaccine.
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Description
Vaccines protect many people from dangerous illnesses, but vaccines, like drugs, can cause side effects, a small percentage of which may be serious. Vaccine Adverse Event Reporting System (VAERS) is used to continually monitor reports to determine whether any vaccine or vaccine lot has a higher than expected rate of events.
Each year the VAERS receives 10,000–20,000 reports of adverse events following immunization by more than 10 million vaccines. Higher-priority uses of the data include reports of death and other serious adverse events, recognizing and detecting adverse effects, and finding unexpected adverse events involving new vaccines. The VAERS data are also used to monitor known reactions to vaccines and for vaccine lot surveillance. Data mining techniques such as empirical Bayes methods can be used to improve the quality of data analysis.
About this Dataset
Data Info
Date Created | 2018 |
---|---|
Last Modified | 2019-08-06 |
Version | 2019-08-06 |
Update Frequency |
Annual |
Temporal Coverage |
2018 |
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 | Adverse Event Reporting System Vaccine Information, VAERS Vaccine Info Data, VAERS Data 2018, Vaccination Reporting System 2018, Vaccine Adverse Event Reporting System VAERS Data, VAERS Data, FDA Vaccine Reports, CDC Vaccine Reports, Vaccine Side Effects |
Other Titles | VAERS Database 2018, Vaccine Adverse Events 2018, Adverse Event Reporting System 2018 |
Data Fields
Name | Description | Type | Constraints |
---|---|---|---|
VAERS_Identification_Number | Unique Vaccine Adverse Event Reporting System Identification Number | integer | level : Nominal |
Administered_Vaccine_Type | Type of administration of vaccines | string | - |
Vaccine_Manufacturer | Manufacturer or company name of vaccine | string | - |
Manufacturer_Vaccine_Lot | Manufacturer's Vaccine Lot Number | string | - |
Previous_Doses_Administered | Number of previous doses administered | integer | level : Ratio |
Vaccination_Route | Vaccination Route | string | - |
Vaccination_Site | Vaccination Site | string | - |
Vaccination_Name | Name of the Vaccination | string | - |
Data Preview
VAERS Identification Number | Administered Vaccine Type | Vaccine Manufacturer | Manufacturer Vaccine Lot | Previous Doses Administered | Vaccination Route | Vaccination Site | Vaccination Name |
732217 | UNK | UNKNOWN MANUFACTURER | VACCINE NOT SPECIFIED (NO BRAND NAME) | ||||
732218 | DTAPIPVHIB | SANOFI PASTEUR | IM | LG | DTAP + IPV + HIB (PENTACEL) | ||
732218 | PPV | UNKNOWN MANUFACTURER | IM | LG | PNEUMO (NO BRAND NAME) | ||
732218 | RV1 | GLAXOSMITHKLINE BIOLOGICALS | PO | MO | ROTAVIRUS (ROTARIX) | ||
732219 | VARZOS | GLAXOSMITHKLINE BIOLOGICALS | 324KL | 1.0 | IM | RA | ZOSTER (SHINGRIX) |
732220 | FLU3 | SANOFI PASTEUR | UI884AB | IM | LA | INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) | |
732221 | ANTH | EMERGENT BIOSOLUTIONS | 300020A | IM | RA | ANTHRAX (BIOTHRAX) | |
732222 | MMR | MERCK & CO. INC. | 1.0 | SYR | RL | MEASLES + MUMPS + RUBELLA (MMR II) | |
732223 | FLU3 | SANOFI PASTEUR | UI897AA | IM | RA | INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) | |
732224 | TDAP | SANOFI PASTEUR | 1.0 | IM | LA | TDAP (ADACEL) |