openfda_significant_adverse_drug_reactions
Identifier
Section titled “Identifier”Description
Section titled “Description”Significant adverse drug reactions (ADRs) associated with drugs.
This dataset is based on the FDA’s Adverse Event Reporting System (FAERS) reporting post-marketing surveillance data and it’s filtered to include only reports submitted by health professionals.
The significance of a given drug-ADR is estimated using a Likelihood Ratio Test (LRT) using all reports associated with the given drug [Drug]
Partitions
Section titled “Partitions”release'26.06'
Schema
Section titled “Schema”| Column | Type | Description |
|---|---|---|
chembl_id |
TEXT |
Unique identifier for the drug or clinical candidate |
event |
TEXT |
Reported adverse drug reaction associated with the drug |
count |
BIGINT |
Number of occurrences of the adverse event in the dataset |
llr |
DOUBLE |
Log-likelihood ratio (LLR) measuring the strength of the association between the drug and the adverse event |
critval |
DOUBLE |
Critical value used to determine statistical significance of the association |
meddraCode |
TEXT |
Medical Dictionary for Regulatory Activities (MedDRA) code for the adverse drug reaction |
release |
TEXT |
Partition column. Open Targets Platform release version (major.minor), e.g. 26.06. [Added during ingest.] |