{
  "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": "16747775",
      "primarysourcecountry": "US",
      "occurcountry": "US",
      "transmissiondateformat": "102",
      "transmissiondate": "20191005",
      "reporttype": "1",
      "serious": "1",
      "seriousnessother": "1",
      "receivedateformat": "102",
      "receivedate": "20190827",
      "receiptdateformat": "102",
      "receiptdate": "20190827",
      "fulfillexpeditecriteria": "2",
      "companynumb": "US-CELGENEUS-USA-20190808229",
      "duplicate": "1",
      "reportduplicate": {
        "duplicatesource": "CELGENE",
        "duplicatenumb": "US-CELGENEUS-USA-20190808229"
      },
      "primarysource": {
        "reportercountry": "US",
        "qualification": "2"
      },
      "sender": {
        "sendertype": "2",
        "senderorganization": "FDA-Public Use"
      },
      "receiver": {
        "receivertype": "6",
        "receiverorganization": "FDA"
      },
      "patient": {
        "patientweight": "66.24",
        "patientsex": "2",
        "reaction": [
          {
            "reactionmeddraversionpt": "22.0",
            "reactionmeddrapt": "Cataract",
            "reactionoutcome": "2"
          }
        ],
        "drug": [
          {
            "drugcharacterization": "2",
            "medicinalproduct": "ATIVAN",
            "drugdosageform": "TABLETS",
            "drugadministrationroute": "048",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "activesubstance": {
              "activesubstancename": "LORAZEPAM"
            },
            "openfda": {
              "application_number": [
                "NDA017794",
                "NDA018140"
              ],
              "brand_name": [
                "ATIVAN"
              ],
              "generic_name": [
                "LORAZEPAM"
              ],
              "manufacturer_name": [
                "Bausch Health US LLC",
                "Hikma Pharmaceuticals USA Inc."
              ],
              "product_ndc": [
                "0187-0063",
                "0187-0064",
                "0187-0065",
                "0641-6000",
                "0641-6003",
                "0641-6002",
                "0641-6001"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL",
                "INTRAMUSCULAR",
                "INTRAVENOUS"
              ],
              "substance_name": [
                "LORAZEPAM"
              ],
              "rxcui": [
                "104719",
                "197900",
                "197901",
                "197902",
                "206821",
                "206828",
                "206819",
                "206820",
                "238100",
                "238101",
                "1665188",
                "1665190",
                "1665326",
                "1665327"
              ],
              "spl_id": [
                "93bdf2de-1222-44a4-b4d5-2280f9ce58d8",
                "209b0091-c890-4f69-a693-d0594c2606fe"
              ],
              "spl_set_id": [
                "89057c93-8155-4040-acec-64e877bd2b4c",
                "5fc0e987-61c9-40c4-b0d5-fcea07c8733e"
              ],
              "package_ndc": [
                "0187-0063-01",
                "0187-0063-50",
                "0187-0063-10",
                "0187-0064-01",
                "0187-0064-50",
                "0187-0064-10",
                "0187-0065-01",
                "0187-0065-50",
                "0187-0065-10",
                "0641-6003-01",
                "0641-6003-25",
                "0641-6002-01",
                "0641-6002-10",
                "0641-6001-01",
                "0641-6001-25",
                "0641-6000-01",
                "0641-6000-10"
              ],
              "nui": [
                "N0000175694",
                "M0002356"
              ],
              "pharm_class_epc": [
                "Benzodiazepine [EPC]"
              ],
              "pharm_class_cs": [
                "Benzodiazepines [CS]"
              ],
              "unii": [
                "O26FZP769L"
              ]
            }
          },
          {
            "drugcharacterization": "1",
            "medicinalproduct": "REVLIMID",
            "drugbatchnumb": "A2869B",
            "drugauthorizationnumb": "021880",
            "drugstructuredosagenumb": "10",
            "drugstructuredosageunit": "003",
            "drugseparatedosagenumb": "1",
            "drugintervaldosageunitnumb": "1",
            "drugintervaldosagedefinition": "804",
            "drugdosagetext": "10 MILLIGRAM",
            "drugdosageform": "CAPSULES",
            "drugadministrationroute": "048",
            "drugindication": "PLASMA CELL MYELOMA",
            "drugstartdateformat": "102",
            "drugstartdate": "20170619",
            "actiondrug": "4",
            "drugrecurreadministration": "3",
            "activesubstance": {
              "activesubstancename": "LENALIDOMIDE"
            },
            "openfda": {
              "application_number": [
                "NDA021880"
              ],
              "brand_name": [
                "REVLIMID"
              ],
              "generic_name": [
                "LENALIDOMIDE"
              ],
              "manufacturer_name": [
                "Celgene Corporation"
              ],
              "product_ndc": [
                "59572-402",
                "59572-405",
                "59572-410",
                "59572-415",
                "59572-420",
                "59572-425"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "LENALIDOMIDE"
              ],
              "rxcui": [
                "602910",
                "602912",
                "616114",
                "616116",
                "643712",
                "643714",
                "643720",
                "643722",
                "1242231",
                "1242233",
                "1428947",
                "1429367"
              ],
              "spl_id": [
                "9329fd28-b848-4013-92e0-a68270328336"
              ],
              "spl_set_id": [
                "5fa97bf5-28a2-48f1-8955-f56012d296be"
              ],
              "package_ndc": [
                "59572-402-28",
                "59572-402-00",
                "59572-405-28",
                "59572-405-00",
                "59572-410-28",
                "59572-410-00",
                "59572-415-21",
                "59572-415-00",
                "59572-420-21",
                "59572-420-00",
                "59572-425-21",
                "59572-425-00"
              ],
              "nui": [
                "N0000184014"
              ],
              "pharm_class_epc": [
                "Thalidomide Analog [EPC]"
              ],
              "unii": [
                "F0P408N6V4"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "MARINOL",
            "drugdosageform": "CAPSULES",
            "drugadministrationroute": "048",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "activesubstance": {
              "activesubstancename": "DRONABINOL"
            },
            "openfda": {
              "application_number": [
                "NDA018651"
              ],
              "brand_name": [
                "MARINOL"
              ],
              "generic_name": [
                "DRONABINOL"
              ],
              "manufacturer_name": [
                "ThePharmaNetwork, LLC"
              ],
              "product_ndc": [
                "53097-568",
                "53097-569",
                "53097-570",
                "53097-571",
                "53097-572",
                "53097-573"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "DRONABINOL"
              ],
              "rxcui": [
                "197634",
                "197635",
                "197636",
                "205641",
                "205642",
                "205645"
              ],
              "spl_id": [
                "628f9609-6583-49be-be77-b64cfbc46fd7",
                "5ce802d5-e8ab-4cd1-9ba0-1f39f22ddd48"
              ],
              "spl_set_id": [
                "628f9609-6583-49be-be77-b64cfbc46fd7",
                "d0efeeec-640d-43c3-8f0a-d31324a11c68"
              ],
              "package_ndc": [
                "53097-568-60",
                "53097-569-60",
                "53097-570-60",
                "53097-571-60",
                "53097-572-60",
                "53097-573-60"
              ],
              "nui": [
                "N0000175782",
                "M0003267"
              ],
              "pharm_class_epc": [
                "Cannabinoid [EPC]"
              ],
              "pharm_class_cs": [
                "Cannabinoids [CS]"
              ],
              "unii": [
                "7J8897W37S"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "CALCIUM D",
            "drugdosagetext": "500MG-1000",
            "drugdosageform": "TABLETS",
            "drugadministrationroute": "048",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "activesubstance": {
              "activesubstancename": "CALCIUM\\VITAMIN D"
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "VALACYCLOVIR HYDROCHLORIDE.",
            "drugdosageform": "UNKNOWN",
            "drugadministrationroute": "065",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "activesubstance": {
              "activesubstancename": "VALACYCLOVIR HYDROCHLORIDE"
            },
            "openfda": {
              "application_number": [
                "NDA020487",
                "ANDA090682",
                "ANDA078518",
                "ANDA201506",
                "ANDA209553",
                "ANDA079012"
              ],
              "brand_name": [
                "VALTREX",
                "VALACYCLOVIR HYDROCHLORIDE",
                "VALACYCLOVIR"
              ],
              "generic_name": [
                "VALACYCLOVIR HYDROCHLORIDE",
                "VALACYCLOVIR"
              ],
              "manufacturer_name": [
                "GlaxoSmithKline LLC",
                "Aurobindo Pharma Limited",
                "NorthStar Rx LLC",
                "Mylan Pharmaceuticals Inc.",
                "Jubilant Cadista Pharmaceuticals Inc.",
                "Yiling Pharmaceutical, Inc.",
                "TIME CAP LABORATORIES, INC.",
                "Rising Pharma Holdings, Inc."
              ],
              "product_ndc": [
                "0173-0565",
                "0173-0933",
                "65862-448",
                "65862-449",
                "16714-697",
                "16714-698",
                "0378-4275",
                "0378-4276",
                "59746-324",
                "59746-325",
                "69117-0011",
                "69117-0010",
                "49483-690",
                "49483-691",
                "57237-042",
                "57237-043"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "VALACYCLOVIR HYDROCHLORIDE"
              ],
              "rxcui": [
                "108780",
                "212448",
                "313564",
                "313565"
              ],
              "spl_id": [
                "861c5801-9c12-4a6b-9bf4-aacb183a58b0",
                "aecf12c1-9094-48b6-8cb0-fcace52e191a",
                "6b2156c4-0d81-4c53-b497-85ed8d7656d0",
                "7de6158d-06ad-4500-a485-dafc151c16ff",
                "40211dd2-c21e-45a4-a8d4-04febf925f52",
                "47237b45-ce93-292b-e063-6394a90a1ab5",
                "c715d9f2-9fe1-0bdd-e053-2a95a90aecf2",
                "a9ee543a-9c63-46df-99f9-cd085ce08bee"
              ],
              "spl_set_id": [
                "f8e0d8f8-cb73-4206-a484-88f5c4fbd719",
                "f5cfb61e-d971-4a9c-b9ef-4f3368fe02f5",
                "4acf51de-26f7-42b2-8acc-61b800627ef3",
                "56bf715d-8280-4557-9f98-9693932199e5",
                "3277c17e-f953-2b0a-fe0a-4f5d1aeace9d",
                "f3ee4017-a4fc-475d-a49b-b39168ec5966",
                "c33a2a36-16d3-4a35-e053-2995a90af240",
                "8d1645c0-fd03-4992-9372-98026a26b3af"
              ],
              "package_ndc": [
                "0173-0933-08",
                "0173-0933-10",
                "0173-0565-04",
                "0173-0565-10",
                "65862-448-30",
                "65862-448-90",
                "65862-448-01",
                "65862-448-05",
                "65862-448-35",
                "65862-448-10",
                "65862-449-30",
                "65862-449-90",
                "65862-449-01",
                "65862-449-05",
                "65862-449-15",
                "16714-698-01",
                "16714-698-03",
                "16714-698-02",
                "16714-697-01",
                "16714-697-03",
                "16714-697-02",
                "16714-697-04",
                "0378-4275-93",
                "0378-4275-77",
                "0378-4276-93",
                "0378-4276-77",
                "59746-324-10",
                "59746-324-30",
                "59746-324-90",
                "59746-324-01",
                "59746-324-37",
                "59746-324-47",
                "59746-325-10",
                "59746-325-30",
                "59746-325-90",
                "59746-325-01",
                "59746-325-37",
                "59746-325-47",
                "69117-0010-1",
                "69117-0010-2",
                "69117-0010-3",
                "69117-0011-1",
                "69117-0011-2",
                "69117-0011-3",
                "49483-690-03",
                "49483-690-41",
                "49483-690-50",
                "49483-690-04",
                "49483-691-03",
                "49483-691-50",
                "49483-691-04",
                "49483-691-01",
                "57237-042-30",
                "57237-042-90",
                "57237-042-05",
                "57237-043-30",
                "57237-043-90",
                "57237-043-05"
              ],
              "unii": [
                "G447S0T1VC"
              ]
            }
          },
          {
            "drugcharacterization": "1",
            "medicinalproduct": "REVLIMID",
            "drugbatchnumb": "A2869B",
            "drugauthorizationnumb": "021880",
            "drugstructuredosagenumb": "5",
            "drugstructuredosageunit": "003",
            "drugdosagetext": "5 MILLIGRAM",
            "drugdosageform": "CAPSULES",
            "drugadministrationroute": "048",
            "drugstartdateformat": "610",
            "drugstartdate": "201709",
            "actiondrug": "4",
            "drugrecurreadministration": "3",
            "activesubstance": {
              "activesubstancename": "LENALIDOMIDE"
            },
            "openfda": {
              "application_number": [
                "NDA021880"
              ],
              "brand_name": [
                "REVLIMID"
              ],
              "generic_name": [
                "LENALIDOMIDE"
              ],
              "manufacturer_name": [
                "Celgene Corporation"
              ],
              "product_ndc": [
                "59572-402",
                "59572-405",
                "59572-410",
                "59572-415",
                "59572-420",
                "59572-425"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "LENALIDOMIDE"
              ],
              "rxcui": [
                "602910",
                "602912",
                "616114",
                "616116",
                "643712",
                "643714",
                "643720",
                "643722",
                "1242231",
                "1242233",
                "1428947",
                "1429367"
              ],
              "spl_id": [
                "9329fd28-b848-4013-92e0-a68270328336"
              ],
              "spl_set_id": [
                "5fa97bf5-28a2-48f1-8955-f56012d296be"
              ],
              "package_ndc": [
                "59572-402-28",
                "59572-402-00",
                "59572-405-28",
                "59572-405-00",
                "59572-410-28",
                "59572-410-00",
                "59572-415-21",
                "59572-415-00",
                "59572-420-21",
                "59572-420-00",
                "59572-425-21",
                "59572-425-00"
              ],
              "nui": [
                "N0000184014"
              ],
              "pharm_class_epc": [
                "Thalidomide Analog [EPC]"
              ],
              "unii": [
                "F0P408N6V4"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "GLUTAMINE",
            "drugdosageform": "POWDER",
            "drugadministrationroute": "065",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "activesubstance": {
              "activesubstancename": "GLUTAMINE"
            },
            "openfda": {
              "application_number": [
                "NDA208587"
              ],
              "brand_name": [
                "ENDARI"
              ],
              "generic_name": [
                "GLUTAMINE"
              ],
              "manufacturer_name": [
                "Emmaus Medical, Inc."
              ],
              "product_ndc": [
                "42457-420"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "GLUTAMINE"
              ],
              "rxcui": [
                "1869684",
                "1928941"
              ],
              "spl_id": [
                "10f5d160-6687-44d5-a607-6bf69a7312b6"
              ],
              "spl_set_id": [
                "d5a783f4-12ef-4326-8faa-40018e45ba3b"
              ],
              "package_ndc": [
                "42457-420-01",
                "42457-420-60"
              ],
              "nui": [
                "N0000175780",
                "M0000922"
              ],
              "pharm_class_epc": [
                "Amino Acid [EPC]"
              ],
              "pharm_class_cs": [
                "Amino Acids [CS]"
              ],
              "unii": [
                "0RH81L854J"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "REMERON",
            "drugdosageform": "TABLETS",
            "drugadministrationroute": "048",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "activesubstance": {
              "activesubstancename": "MIRTAZAPINE"
            },
            "openfda": {
              "application_number": [
                "NDA020415"
              ],
              "brand_name": [
                "REMERON"
              ],
              "generic_name": [
                "MIRTAZAPINE"
              ],
              "manufacturer_name": [
                "Organon LLC"
              ],
              "product_ndc": [
                "78206-160",
                "78206-161",
                "78206-156",
                "78206-158",
                "78206-159"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "MIRTAZAPINE"
              ],
              "rxcui": [
                "211322",
                "211323",
                "283406",
                "283407",
                "283485",
                "311725",
                "314111",
                "752869",
                "752870",
                "752871"
              ],
              "spl_id": [
                "8b121c7c-9bcd-4504-b789-3f551a0fe514"
              ],
              "spl_set_id": [
                "98ad1917-a094-44f5-a28f-a64a8cfcd887"
              ],
              "package_ndc": [
                "78206-160-01",
                "78206-161-01",
                "78206-156-99",
                "78206-156-01",
                "78206-158-99",
                "78206-158-01",
                "78206-159-99",
                "78206-159-01"
              ],
              "unii": [
                "A051Q2099Q"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "ZINC-15",
            "drugdosageform": "TABLETS",
            "drugadministrationroute": "048",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION"
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "PREVACID",
            "drugdosageform": "TABLETS",
            "drugadministrationroute": "048",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "activesubstance": {
              "activesubstancename": "LANSOPRAZOLE"
            },
            "openfda": {
              "application_number": [
                "NDA020406"
              ],
              "brand_name": [
                "PREVACID"
              ],
              "generic_name": [
                "LANSOPRAZOLE"
              ],
              "manufacturer_name": [
                "Takeda Pharmaceuticals America, Inc."
              ],
              "product_ndc": [
                "64764-046",
                "64764-543",
                "64764-544"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "LANSOPRAZOLE"
              ],
              "rxcui": [
                "206205",
                "206206",
                "311277",
                "351260",
                "351261",
                "866152"
              ],
              "spl_id": [
                "45f1d5ff-d884-4e40-a16c-313a4e21e32c"
              ],
              "spl_set_id": [
                "71ba78cb-7e46-43eb-9425-fa130f537f84"
              ],
              "package_ndc": [
                "64764-046-13",
                "64764-046-19",
                "64764-046-11",
                "64764-046-06",
                "64764-543-30",
                "64764-543-11",
                "64764-543-05",
                "64764-544-30",
                "64764-544-11",
                "64764-544-05"
              ],
              "nui": [
                "N0000175525",
                "N0000000147",
                "N0000009724"
              ],
              "pharm_class_epc": [
                "Proton Pump Inhibitor [EPC]"
              ],
              "pharm_class_moa": [
                "Proton Pump Inhibitors [MoA]"
              ],
              "pharm_class_pe": [
                "Inhibition Gastric Acid Secretion [PE]"
              ],
              "unii": [
                "0K5C5T2QPG"
              ]
            }
          },
          {
            "drugcharacterization": "1",
            "medicinalproduct": "REVLIMID",
            "drugbatchnumb": "A2869B",
            "drugauthorizationnumb": "021880",
            "drugstructuredosagenumb": "25",
            "drugstructuredosageunit": "003",
            "drugseparatedosagenumb": "1",
            "drugintervaldosageunitnumb": "1",
            "drugintervaldosagedefinition": "804",
            "drugdosagetext": "25 MILLIGRAM",
            "drugdosageform": "CAPSULES",
            "drugadministrationroute": "048",
            "drugindication": "PLASMA CELL LEUKAEMIA",
            "drugstartdateformat": "610",
            "drugstartdate": "201612",
            "actiondrug": "4",
            "drugrecurreadministration": "3",
            "activesubstance": {
              "activesubstancename": "LENALIDOMIDE"
            },
            "openfda": {
              "application_number": [
                "NDA021880"
              ],
              "brand_name": [
                "REVLIMID"
              ],
              "generic_name": [
                "LENALIDOMIDE"
              ],
              "manufacturer_name": [
                "Celgene Corporation"
              ],
              "product_ndc": [
                "59572-402",
                "59572-405",
                "59572-410",
                "59572-415",
                "59572-420",
                "59572-425"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "LENALIDOMIDE"
              ],
              "rxcui": [
                "602910",
                "602912",
                "616114",
                "616116",
                "643712",
                "643714",
                "643720",
                "643722",
                "1242231",
                "1242233",
                "1428947",
                "1429367"
              ],
              "spl_id": [
                "9329fd28-b848-4013-92e0-a68270328336"
              ],
              "spl_set_id": [
                "5fa97bf5-28a2-48f1-8955-f56012d296be"
              ],
              "package_ndc": [
                "59572-402-28",
                "59572-402-00",
                "59572-405-28",
                "59572-405-00",
                "59572-410-28",
                "59572-410-00",
                "59572-415-21",
                "59572-415-00",
                "59572-420-21",
                "59572-420-00",
                "59572-425-21",
                "59572-425-00"
              ],
              "nui": [
                "N0000184014"
              ],
              "pharm_class_epc": [
                "Thalidomide Analog [EPC]"
              ],
              "unii": [
                "F0P408N6V4"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "KLONOPIN",
            "drugdosageform": "TABLETS",
            "drugadministrationroute": "048",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "activesubstance": {
              "activesubstancename": "CLONAZEPAM"
            },
            "openfda": {
              "application_number": [
                "NDA017533"
              ],
              "brand_name": [
                "KLONOPIN"
              ],
              "generic_name": [
                "CLONAZEPAM"
              ],
              "manufacturer_name": [
                "H2-Pharma, LLC"
              ],
              "product_ndc": [
                "61269-605",
                "61269-610",
                "61269-620"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "CLONAZEPAM"
              ],
              "rxcui": [
                "197527",
                "197528",
                "197529",
                "206157",
                "206159",
                "206160"
              ],
              "spl_id": [
                "63cfdab9-fb3d-4c2b-bf88-8ba841dba839"
              ],
              "spl_set_id": [
                "cfa0d79a-843c-4b88-95a1-e9511d649ca1"
              ],
              "package_ndc": [
                "61269-605-10",
                "61269-610-10",
                "61269-620-10"
              ],
              "nui": [
                "N0000175694",
                "M0002356"
              ],
              "pharm_class_epc": [
                "Benzodiazepine [EPC]"
              ],
              "pharm_class_cs": [
                "Benzodiazepines [CS]"
              ],
              "unii": [
                "5PE9FDE8GB"
              ]
            }
          }
        ]
      }
    }
  ]
}