{
  "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": "2026-04-28",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 111630
    }
  },
  "results": [
    {
      "safetyreportversion": "1",
      "safetyreportid": "10003512",
      "primarysourcecountry": "JP",
      "occurcountry": "JP",
      "transmissiondateformat": "102",
      "transmissiondate": "20141002",
      "reporttype": "1",
      "serious": "1",
      "seriousnesshospitalization": "1",
      "receivedateformat": "102",
      "receivedate": "20140312",
      "receiptdateformat": "102",
      "receiptdate": "20140312",
      "fulfillexpeditecriteria": "1",
      "companynumb": "JP-ELI_LILLY_AND_COMPANY-JP201403001062",
      "duplicate": "1",
      "reportduplicate": {
        "duplicatesource": "ELI LILLY AND CO",
        "duplicatenumb": "JP-ELI_LILLY_AND_COMPANY-JP201403001062"
      },
      "primarysource": {
        "reportercountry": "JP",
        "qualification": "5"
      },
      "sender": {
        "sendertype": "2",
        "senderorganization": "FDA-Public Use"
      },
      "receiver": {
        "receivertype": "6",
        "receiverorganization": "FDA"
      },
      "patient": {
        "patientonsetage": "75",
        "patientonsetageunit": "801",
        "patientsex": "1",
        "reaction": [
          {
            "reactionmeddraversionpt": "17.0",
            "reactionmeddrapt": "Femur fracture",
            "reactionoutcome": "3"
          },
          {
            "reactionmeddraversionpt": "17.0",
            "reactionmeddrapt": "Fall",
            "reactionoutcome": "1"
          }
        ],
        "drug": [
          {
            "drugcharacterization": "1",
            "medicinalproduct": "FORTEO",
            "drugauthorizationnumb": "021318",
            "drugdosagetext": "UNK",
            "drugdosageform": "INJECTION",
            "drugadministrationroute": "058",
            "drugindication": "OSTEOPOROSIS",
            "drugstartdateformat": "610",
            "drugstartdate": "201309",
            "actiondrug": "4",
            "openfda": {
              "application_number": [
                "NDA021318"
              ],
              "brand_name": [
                "FORTEO"
              ],
              "generic_name": [
                "TERIPARATIDE"
              ],
              "manufacturer_name": [
                "Eli Lilly and Company"
              ],
              "product_ndc": [
                "0002-8400",
                "0002-9678"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "SUBCUTANEOUS"
              ],
              "substance_name": [
                "TERIPARATIDE"
              ],
              "rxcui": [
                "1435115",
                "1435117"
              ],
              "spl_id": [
                "31aeb334-c6d1-4018-af85-17ef69850001"
              ],
              "spl_set_id": [
                "aae667c5-381f-4f92-93df-2ed6158d07b0"
              ],
              "package_ndc": [
                "0002-8400-01",
                "0002-9678-01"
              ],
              "nui": [
                "M0015931",
                "N0000180852"
              ],
              "pharm_class_cs": [
                "Parathyroid Hormone [CS]"
              ],
              "pharm_class_epc": [
                "Parathyroid Hormone Analog [EPC]"
              ],
              "unii": [
                "10T9CSU89I"
              ]
            }
          }
        ]
      }
    }
  ]
}