{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-30",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "safetyreportversion": "1",
      "safetyreportid": "16989027",
      "primarysourcecountry": "US",
      "occurcountry": "US",
      "transmissiondateformat": "102",
      "transmissiondate": "20200122",
      "reporttype": "1",
      "serious": "1",
      "seriousnesshospitalization": "1",
      "receivedateformat": "102",
      "receivedate": "20191104",
      "receiptdateformat": "102",
      "receiptdate": "20191104",
      "fulfillexpeditecriteria": "1",
      "companynumb": "US-GW PHARMA-201910USGW3985",
      "duplicate": "1",
      "reportduplicate": {
        "duplicatesource": "GW PHARMA",
        "duplicatenumb": "US-GW PHARMA-201910USGW3985"
      },
      "primarysource": {
        "reportercountry": "US",
        "qualification": "3"
      },
      "sender": {
        "sendertype": "2",
        "senderorganization": "FDA-Public Use"
      },
      "receiver": {
        "receivertype": "6",
        "receiverorganization": "FDA"
      },
      "patient": {
        "reaction": [
          {
            "reactionmeddraversionpt": "22.1",
            "reactionmeddrapt": "Seizure",
            "reactionoutcome": "3"
          }
        ],
        "drug": [
          {
            "drugcharacterization": "1",
            "medicinalproduct": "EPIDIOLEX",
            "drugbatchnumb": "W002951",
            "drugstructuredosagenumb": "300",
            "drugstructuredosageunit": "003",
            "drugdosagetext": "300 MILLIGRAM, BID",
            "drugdosageform": "ORAL SOLUTION",
            "drugadministrationroute": "048",
            "drugindication": "EPILEPSY",
            "drugstartdateformat": "102",
            "drugstartdate": "20190209",
            "actiondrug": "4",
            "activesubstance": {
              "activesubstancename": "CANNABIDIOL"
            },
            "openfda": {
              "application_number": [
                "NDA210365"
              ],
              "brand_name": [
                "EPIDIOLEX"
              ],
              "generic_name": [
                "CANNABIDIOL"
              ],
              "manufacturer_name": [
                "Jazz Pharmaceuticals, Inc."
              ],
              "product_ndc": [
                "70127-100"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "CANNABIDIOL"
              ],
              "rxcui": [
                "2058900",
                "2058906"
              ],
              "spl_id": [
                "1eb7ac65-8df5-4a4a-9156-802cfaa92b06"
              ],
              "spl_set_id": [
                "8bf27097-4870-43fb-94f0-f3d0871d1eec"
              ],
              "package_ndc": [
                "70127-100-01",
                "70127-100-10",
                "70127-100-06",
                "70127-100-60"
              ],
              "nui": [
                "M0003267",
                "N0000187062",
                "N0000185504",
                "N0000182140",
                "N0000191278",
                "N0000191273",
                "N0000182138",
                "N0000182139",
                "N0000187064"
              ],
              "pharm_class_cs": [
                "Cannabinoids [CS]"
              ],
              "pharm_class_moa": [
                "Cytochrome P450 2C8 Inhibitors [MoA]",
                "Cytochrome P450 2C9 Inhibitors [MoA]",
                "Cytochrome P450 2C19 Inhibitors [MoA]",
                "UGT1A9 Inhibitors [MoA]",
                "UGT2B7 Inhibitors [MoA]",
                "Cytochrome P450 1A2 Inhibitors [MoA]",
                "Cytochrome P450 2B6 Inhibitors [MoA]",
                "Cytochrome P450 2B6 Inducers [MoA]"
              ],
              "unii": [
                "19GBJ60SN5"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "POLYETHYLENE GLYCOL",
            "drugdosagetext": "UNK",
            "drugadministrationroute": "065",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "activesubstance": {
              "activesubstancename": "POLYETHYLENE GLYCOLS"
            },
            "openfda": {
              "application_number": [
                "M018",
                "ANDA091077"
              ],
              "brand_name": [
                "RETAINE ULTRA PF",
                "POLYETHYLENE GLYCOL"
              ],
              "generic_name": [
                "POLYETHYLENE GLYCOL"
              ],
              "manufacturer_name": [
                "OCuSOFT LLC",
                "BluePoint Laboratories"
              ],
              "product_ndc": [
                "54799-470",
                "68001-505"
              ],
              "product_type": [
                "HUMAN OTC DRUG"
              ],
              "route": [
                "OPHTHALMIC",
                "ORAL"
              ],
              "substance_name": [
                "POLYETHYLENE GLYCOL 400",
                "PROPYLENE GLYCOL",
                "POLYETHYLENE GLYCOL 3350"
              ],
              "rxcui": [
                "477589"
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              "spl_id": [
                "73f4c537-3cc4-49cd-a580-9adfb7e5f4fb",
                "cc6e2865-14e2-1ac7-e053-2a95a90acbc0"
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              "spl_set_id": [
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                "c4cae70c-68da-0bbc-e053-2a95a90a395a"
              ],
              "package_ndc": [
                "54799-470-10",
                "68001-505-55",
                "68001-505-69"
              ],
              "unii": [
                "B697894SGQ",
                "6DC9Q167V3",
                "G2M7P15E5P"
              ],
              "nui": [
                "N0000010288",
                "N0000175811",
                "N0000009871"
              ],
              "pharm_class_moa": [
                "Osmotic Activity [MoA]"
              ],
              "pharm_class_epc": [
                "Osmotic Laxative [EPC]"
              ],
              "pharm_class_pe": [
                "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"
              ]
            }
          }
        ],
        "summary": {
          "narrativeincludeclinical": "CASE EVENT DATE: 20191015"
        }
      }
    }
  ]
}