{
  "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": 4
    }
  },
  "results": [
    {
      "safetyreportversion": "2",
      "safetyreportid": "22169610",
      "primarysourcecountry": "US",
      "occurcountry": "US",
      "transmissiondateformat": "102",
      "transmissiondate": "20230721",
      "reporttype": "2",
      "serious": "1",
      "seriousnessdeath": "2",
      "seriousnesslifethreatening": "2",
      "seriousnesshospitalization": "1",
      "seriousnessdisabling": "2",
      "seriousnesscongenitalanomali": "2",
      "seriousnessother": "2",
      "receivedateformat": "102",
      "receivedate": "20230404",
      "receiptdateformat": "102",
      "receiptdate": "20230421",
      "fulfillexpeditecriteria": "1",
      "companynumb": "US-NOVOPROD-1043796",
      "primarysource": {
        "reportercountry": "US",
        "qualification": "1"
      },
      "sender": {
        "sendertype": "2",
        "senderorganization": "FDA-Public Use"
      },
      "receiver": {
        "receivertype": "6",
        "receiverorganization": "FDA"
      },
      "patient": {
        "patientonsetage": "56",
        "patientonsetageunit": "801",
        "patientweight": "103",
        "patientsex": "2",
        "reaction": [
          {
            "reactionmeddraversionpt": "26.0",
            "reactionmeddrapt": "Gastroenteritis",
            "reactionoutcome": "1"
          }
        ],
        "drug": [
          {
            "drugcharacterization": "1",
            "medicinalproduct": "SEMAGLUTIDE",
            "drugauthorizationnumb": "215256",
            "drugstructuredosagenumb": "0.5",
            "drugstructuredosageunit": "003",
            "drugseparatedosagenumb": "1",
            "drugintervaldosageunitnumb": "1",
            "drugintervaldosagedefinition": "803",
            "drugdosagetext": "0.5,MG,ONCE PER WEEK",
            "drugdosageform": "Solution for injection",
            "drugadministrationroute": "058",
            "drugindication": "Non-alcoholic steatohepatitis",
            "drugstartdateformat": "102",
            "drugstartdate": "20221006",
            "actiondrug": "4",
            "activesubstance": {
              "activesubstancename": "SEMAGLUTIDE"
            },
            "openfda": {}
          },
          {
            "drugcharacterization": "1",
            "medicinalproduct": "CAGRILINTIDE",
            "drugstructuredosagenumb": "0.5",
            "drugstructuredosageunit": "003",
            "drugseparatedosagenumb": "1",
            "drugintervaldosageunitnumb": "1",
            "drugintervaldosagedefinition": "803",
            "drugdosagetext": "0.5,MG,ONCE PER WEEK",
            "drugdosageform": "Solution for injection",
            "drugadministrationroute": "058",
            "drugindication": "Non-alcoholic steatohepatitis",
            "drugstartdateformat": "102",
            "drugstartdate": "20221006",
            "actiondrug": "4",
            "activesubstance": {
              "activesubstancename": "CAGRILINTIDE"
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "ISOVUE 370",
            "drugdosagetext": "75.0,CC,ONCE",
            "drugindication": "Scan with contrast",
            "drugstartdateformat": "102",
            "drugstartdate": "20230305",
            "drugenddateformat": "102",
            "drugenddate": "20230305",
            "activesubstance": {
              "activesubstancename": "IOPAMIDOL"
            },
            "openfda": {
              "application_number": [
                "NDA020327",
                "NDA018735"
              ],
              "brand_name": [
                "ISOVUE 300",
                "ISOVUE 370",
                "ISOVUE 200",
                "ISOVUE 250"
              ],
              "generic_name": [
                "IOPAMIDOL"
              ],
              "manufacturer_name": [
                "Bracco Diagnostics Inc",
                "BRACCO DIAGNOSTICS INC"
              ],
              "product_ndc": [
                "0270-1315",
                "0270-1316",
                "0270-1314",
                "0270-1317"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "INTRAVASCULAR"
              ],
              "substance_name": [
                "IOPAMIDOL"
              ],
              "spl_id": [
                "c31a9ece-7b14-abe3-6214-f4e8c482516c",
                "2cb2e0be-08b1-e446-01c5-b1c50f1e797c"
              ],
              "spl_set_id": [
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                "ae8c18c9-3e7d-4515-b980-120025a88fc1"
              ],
              "package_ndc": [
                "0270-1315-45",
                "0270-1315-95",
                "0270-1316-45",
                "0270-1316-95",
                "0270-1315-50",
                "0270-1315-25",
                "0270-1315-30",
                "0270-1315-35",
                "0270-1316-52",
                "0270-1316-35",
                "0270-1316-04",
                "0270-1316-37",
                "0270-1316-30",
                "0270-1314-15",
                "0270-1317-02"
              ],
              "nui": [
                "N0000180185",
                "N0000010258"
              ],
              "pharm_class_epc": [
                "Radiographic Contrast Agent [EPC]"
              ],
              "pharm_class_moa": [
                "X-Ray Contrast Activity [MoA]"
              ],
              "unii": [
                "JR13W81H44"
              ]
            }
          }
        ],
        "summary": {
          "narrativeincludeclinical": "CASE EVENT DATE: 20230305"
        }
      }
    }
  ]
}