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openfda

Correlating the OpenFDA Pharmacy Drugs and Reactions based on Adverse Events

Overview

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore a casual relationsip cannot be established between product and reactions listed in a report.

Case Study

Focused on Elderly Patients that have reported serious conditions with hypertension. Hypertension was chosen due to the large number of adverse reports available in contrast to other conditions. At some point in time, while taking multiple prescribed drugs, they have indicated one of the drugs was for hypertension.

  • serious:1
  • patient.patientonsetage:[65+TO+99]
  • patient.drug.drugindication:hypertension

Datasets

  • openFDA
    • Adverse Events
    • Recalls (Certain Recalls of FDA Regulated Products)
    • Labeling

ML Aspects

  • Data Munging, Scaling
  • RBM (Restricted Boltzmann Machine) - Neural Networks (Single Layer)
  • Cosine Similarity

Resources

Neural Networks

Reference Sites

External Source

Usage

  • File Access: ipython test_vectors.py
  • Restful OpenFDA API: ipython test_vectors.py -- -f 0
  • Note that Github prevents large files to be uploaded, so a reference small data sample is provided, more data samples can be retrieved via Restful API.

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Correlating the OpenFDA Pharmacy Drugs and Reactions based on Adverse Events

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