{
  "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": 10393
    }
  },
  "results": [
    {
      "safetyreportversion": "1",
      "safetyreportid": "10006365",
      "primarysourcecountry": "US",
      "occurcountry": "US",
      "transmissiondateformat": "102",
      "transmissiondate": "20141002",
      "reporttype": "1",
      "serious": "1",
      "seriousnessother": "1",
      "receivedateformat": "102",
      "receivedate": "20140313",
      "receiptdateformat": "102",
      "receiptdate": "20140313",
      "fulfillexpeditecriteria": "1",
      "companynumb": "US-PFIZER INC-2014068827",
      "duplicate": "1",
      "reportduplicate": {
        "duplicatesource": "PFIZER",
        "duplicatenumb": "US-PFIZER INC-2014068827"
      },
      "primarysource": {
        "reportercountry": "US",
        "qualification": "5"
      },
      "sender": {
        "sendertype": "2",
        "senderorganization": "FDA-Public Use"
      },
      "receiver": {
        "receivertype": "6",
        "receiverorganization": "FDA"
      },
      "patient": {
        "patientsex": "2",
        "reaction": [
          {
            "reactionmeddraversionpt": "17.0",
            "reactionmeddrapt": "Coeliac disease",
            "reactionoutcome": "6"
          }
        ],
        "drug": [
          {
            "drugcharacterization": "1",
            "medicinalproduct": "TOVIAZ",
            "drugauthorizationnumb": "022030",
            "drugdosagetext": "UNK",
            "drugdosageform": "MODIFIED-RELEASE TABLET",
            "actiondrug": "5",
            "openfda": {
              "application_number": [
                "NDA022030"
              ],
              "brand_name": [
                "TOVIAZ"
              ],
              "generic_name": [
                "FESOTERODINE FUMARATE"
              ],
              "manufacturer_name": [
                "Pfizer Laboratories Div Pfizer Inc"
              ],
              "product_ndc": [
                "0069-0242",
                "0069-0244"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "FESOTERODINE FUMARATE"
              ],
              "rxcui": [
                "810071",
                "810075",
                "810077",
                "810079"
              ],
              "spl_id": [
                "ca2031f1-5425-4d31-bf14-c865ec4e89b7"
              ],
              "spl_set_id": [
                "5be745f0-8ae7-4c3c-9962-37d6263326f1"
              ],
              "package_ndc": [
                "0069-0242-30",
                "0069-0244-30"
              ],
              "unii": [
                "EOS72165S7"
              ]
            }
          },
          {
            "drugcharacterization": "1",
            "medicinalproduct": "DETROL LA",
            "drugauthorizationnumb": "021228",
            "drugdosagetext": "UNK",
            "drugdosageform": "MODIFIED-RELEASE CAPSULE, SOFT",
            "actiondrug": "5",
            "openfda": {
              "application_number": [
                "NDA021228"
              ],
              "brand_name": [
                "DETROL LA"
              ],
              "generic_name": [
                "TOLTERODINE TARTRATE"
              ],
              "manufacturer_name": [
                "Viatris Specialty LLC"
              ],
              "product_ndc": [
                "58151-103",
                "58151-104"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "TOLTERODINE TARTRATE"
              ],
              "rxcui": [
                "855182",
                "855184",
                "855189",
                "855191"
              ],
              "spl_id": [
                "0ca22b08-46d1-4b6f-b9e7-d6a5dd534a1c"
              ],
              "spl_set_id": [
                "d7274947-4f88-47ee-a39f-bd5ac46fcf8d"
              ],
              "package_ndc": [
                "58151-103-93",
                "58151-103-77",
                "58151-103-05",
                "58151-104-93",
                "58151-104-77",
                "58151-104-05"
              ],
              "unii": [
                "5T619TQR3R"
              ]
            }
          }
        ]
      }
    }
  ]
}