{
  "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": 3
    }
  },
  "results": [
    {
      "safetyreportversion": "1",
      "safetyreportid": "24287923",
      "primarysourcecountry": "US",
      "transmissiondateformat": "102",
      "transmissiondate": "20241017",
      "reporttype": "1",
      "serious": "2",
      "seriousnessdeath": "2",
      "seriousnesslifethreatening": "2",
      "seriousnesshospitalization": "2",
      "seriousnessdisabling": "2",
      "seriousnesscongenitalanomali": "2",
      "seriousnessother": "2",
      "receivedateformat": "102",
      "receivedate": "20240905",
      "receiptdateformat": "102",
      "receiptdate": "20240905",
      "fulfillexpeditecriteria": "3",
      "authoritynumb": "717243",
      "primarysource": {
        "reportercountry": "US",
        "qualification": "5"
      },
      "sender": {
        "sendertype": "6",
        "senderorganization": "Public"
      },
      "receiver": {
        "receivertype": "6",
        "receiverorganization": "FDA"
      },
      "patient": {
        "patientonsetage": "76",
        "patientonsetageunit": "801",
        "patientweight": "54",
        "patientsex": "2",
        "reaction": [
          {
            "reactionmeddraversionpt": "27.0",
            "reactionmeddrapt": "Gastrointestinal disorder"
          },
          {
            "reactionmeddraversionpt": "27.0",
            "reactionmeddrapt": "Drug abuser"
          },
          {
            "reactionmeddraversionpt": "27.0",
            "reactionmeddrapt": "Product prescribing issue"
          }
        ],
        "drug": [
          {
            "drugcharacterization": "1",
            "medicinalproduct": "SEMAGLUTIDE",
            "drugauthorizationnumb": "99",
            "drugindication": "Decreased appetite",
            "drugtreatmentduration": "2023",
            "drugtreatmentdurationunit": "801",
            "drugrecurreadministration": "1",
            "drugadditional": "2",
            "activesubstance": {
              "activesubstancename": "SEMAGLUTIDE"
            },
            "openfda": {}
          },
          {
            "drugcharacterization": "1",
            "medicinalproduct": "SEMAGLUTIDE",
            "drugauthorizationnumb": "99",
            "drugindication": "Dependence",
            "drugrecurreadministration": "1",
            "drugadditional": "2",
            "activesubstance": {
              "activesubstancename": "SEMAGLUTIDE"
            },
            "openfda": {}
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "TESOFENSINE",
            "activesubstance": {
              "activesubstancename": "TESOFENSINE"
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "PHENTERMINE",
            "activesubstance": {
              "activesubstancename": "PHENTERMINE\\PHENTERMINE HYDROCHLORIDE"
            },
            "openfda": {
              "application_number": [
                "ANDA204318"
              ],
              "brand_name": [
                "PHENTERMINE"
              ],
              "generic_name": [
                "PHENTERMINE HYDROCHLORIDE"
              ],
              "manufacturer_name": [
                "Aurolife Pharma, LLC"
              ],
              "product_ndc": [
                "13107-105",
                "13107-106"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "PHENTERMINE HYDROCHLORIDE"
              ],
              "rxcui": [
                "900038",
                "968766"
              ],
              "spl_id": [
                "53dd7857-41fb-4da1-88f7-5c68a509bfb0"
              ],
              "spl_set_id": [
                "737eef3b-9a6b-4ab3-a25c-49d84d2a0197"
              ],
              "package_ndc": [
                "13107-105-30",
                "13107-105-01",
                "13107-106-30",
                "13107-106-01"
              ],
              "unii": [
                "0K2I505OTV"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "PEPCID",
            "activesubstance": {
              "activesubstancename": "FAMOTIDINE"
            },
            "openfda": {
              "application_number": [
                "ANDA075805"
              ],
              "brand_name": [
                "PEPCID"
              ],
              "generic_name": [
                "FAMOTIDINE"
              ],
              "manufacturer_name": [
                "Bausch Health US LLC"
              ],
              "product_ndc": [
                "0187-4420",
                "0187-4440"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "FAMOTIDINE"
              ],
              "rxcui": [
                "104094",
                "104095",
                "284245",
                "310273"
              ],
              "spl_id": [
                "7d2d8240-b53a-4395-bd8d-d326522d5865"
              ],
              "spl_set_id": [
                "a06502d9-7903-4f37-833e-e5763d502def"
              ],
              "package_ndc": [
                "0187-4420-30",
                "0187-4420-10",
                "0187-4440-30",
                "0187-4440-10"
              ],
              "nui": [
                "N0000000151",
                "N0000175784"
              ],
              "pharm_class_moa": [
                "Histamine H2 Receptor Antagonists [MoA]"
              ],
              "pharm_class_epc": [
                "Histamine-2 Receptor Antagonist [EPC]"
              ],
              "unii": [
                "5QZO15J2Z8"
              ]
            }
          }
        ],
        "summary": {
          "narrativeincludeclinical": "CASE EVENT DATE: 20240905"
        }
      }
    }
  ]
}