{
  "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": "2",
      "safetyreportid": "14767761",
      "primarysourcecountry": "US",
      "occurcountry": "US",
      "transmissiondateformat": "102",
      "transmissiondate": "20180711",
      "reporttype": "2",
      "serious": "1",
      "seriousnesshospitalization": "1",
      "seriousnessother": "1",
      "receivedateformat": "102",
      "receivedate": "20180417",
      "receiptdateformat": "102",
      "receiptdate": "20180509",
      "fulfillexpeditecriteria": "1",
      "companynumb": "US-TESARO, INC.-US-2018TSO00528",
      "duplicate": "1",
      "reportduplicate": {
        "duplicatesource": "TESARO",
        "duplicatenumb": "US-TESARO, INC.-US-2018TSO00528"
      },
      "primarysource": {
        "reportercountry": "US",
        "qualification": "5"
      },
      "sender": {
        "sendertype": "2",
        "senderorganization": "FDA-Public Use"
      },
      "receiver": {
        "receivertype": "6",
        "receiverorganization": "FDA"
      },
      "patient": {
        "reaction": [
          {
            "reactionmeddraversionpt": "21.0",
            "reactionmeddrapt": "Lung neoplasm malignant",
            "reactionoutcome": "6"
          },
          {
            "reactionmeddraversionpt": "21.0",
            "reactionmeddrapt": "Carbohydrate antigen 125 increased",
            "reactionoutcome": "6"
          },
          {
            "reactionmeddraversionpt": "21.0",
            "reactionmeddrapt": "Drug ineffective",
            "reactionoutcome": "6"
          },
          {
            "reactionmeddraversionpt": "21.0",
            "reactionmeddrapt": "Dysphagia",
            "reactionoutcome": "6"
          },
          {
            "reactionmeddraversionpt": "21.0",
            "reactionmeddrapt": "Stress",
            "reactionoutcome": "6"
          }
        ],
        "drug": [
          {
            "drugcharacterization": "1",
            "medicinalproduct": "ZEJULA",
            "drugauthorizationnumb": "208447",
            "drugstructuredosagenumb": "200",
            "drugstructuredosageunit": "003",
            "drugdosagetext": "200 MG, QD",
            "drugdosageform": "CAPSULE",
            "drugadministrationroute": "048",
            "drugindication": "OVARIAN CANCER",
            "drugstartdateformat": "102",
            "drugstartdate": "20170623",
            "actiondrug": "1",
            "activesubstance": {
              "activesubstancename": "NIRAPARIB"
            },
            "openfda": {
              "application_number": [
                "NDA214876"
              ],
              "brand_name": [
                "ZEJULA"
              ],
              "generic_name": [
                "NIRAPARIB"
              ],
              "manufacturer_name": [
                "GlaxoSmithKline LLC"
              ],
              "product_ndc": [
                "0173-0909",
                "0173-0912",
                "0173-0915"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "NIRAPARIB TOSYLATE"
              ],
              "rxcui": [
                "2637449",
                "2637452",
                "2637465",
                "2640210",
                "2640212",
                "2640214"
              ],
              "spl_id": [
                "b5e85656-77f8-405d-982e-c3d890a0f99b"
              ],
              "spl_set_id": [
                "b7f675e2-159c-490c-b6f4-3f16d9492b7d"
              ],
              "package_ndc": [
                "0173-0909-13",
                "0173-0912-13",
                "0173-0912-61",
                "0173-0915-13",
                "0173-0915-61"
              ],
              "unii": [
                "195Q483UZD"
              ]
            }
          },
          {
            "drugcharacterization": "1",
            "medicinalproduct": "ZEJULA",
            "drugbatchnumb": "5905797",
            "drugauthorizationnumb": "208447",
            "drugstructuredosagenumb": "200",
            "drugstructuredosageunit": "003",
            "drugdosagetext": "200 MG, QD",
            "drugdosageform": "CAPSULE",
            "drugadministrationroute": "048",
            "drugstartdateformat": "102",
            "drugstartdate": "20170723",
            "drugenddateformat": "102",
            "drugenddate": "20180323",
            "actiondrug": "1",
            "activesubstance": {
              "activesubstancename": "NIRAPARIB"
            },
            "openfda": {
              "application_number": [
                "NDA214876"
              ],
              "brand_name": [
                "ZEJULA"
              ],
              "generic_name": [
                "NIRAPARIB"
              ],
              "manufacturer_name": [
                "GlaxoSmithKline LLC"
              ],
              "product_ndc": [
                "0173-0909",
                "0173-0912",
                "0173-0915"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "NIRAPARIB TOSYLATE"
              ],
              "rxcui": [
                "2637449",
                "2637452",
                "2637465",
                "2640210",
                "2640212",
                "2640214"
              ],
              "spl_id": [
                "b5e85656-77f8-405d-982e-c3d890a0f99b"
              ],
              "spl_set_id": [
                "b7f675e2-159c-490c-b6f4-3f16d9492b7d"
              ],
              "package_ndc": [
                "0173-0909-13",
                "0173-0912-13",
                "0173-0912-61",
                "0173-0915-13",
                "0173-0915-61"
              ],
              "unii": [
                "195Q483UZD"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "BIOTIN",
            "drugdosagetext": "UNK",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "actiondrug": "6",
            "activesubstance": {
              "activesubstancename": "BIOTIN"
            },
            "openfda": {
              "application_number": [
                "M032"
              ],
              "brand_name": [
                "AVEYA BIOTIN HAIR GROWTH",
                "BIOTIN",
                "SEVICH CHEBE HAIR"
              ],
              "generic_name": [
                "BIOTIN"
              ],
              "manufacturer_name": [
                "Guangdong Aimu Biological Technology Co., Ltd",
                "Shenzhen yuehaotong Technology Co.,Ltd",
                "Guangzhou Sanwich Biology Technology Co., Ltd"
              ],
              "product_ndc": [
                "83566-561",
                "87492-002",
                "87655-001"
              ],
              "product_type": [
                "HUMAN OTC DRUG"
              ],
              "route": [
                "TOPICAL"
              ],
              "substance_name": [
                "BIOTIN",
                "MINOXIDIL",
                "MACADAMIA TERNIFOLIA SEED OIL",
                "CALENDULA OFFICINALIS SEED OIL"
              ],
              "spl_id": [
                "460fff55-728b-9c3a-e063-6394a90a3188",
                "4c6ec616-a84f-6e1a-e063-6294a90a2aae",
                "55b0b7f8-5ac2-f325-e063-6294a90a0b16"
              ],
              "spl_set_id": [
                "460fff55-728a-9c3a-e063-6394a90a3188",
                "4c6ec616-a84e-6e1a-e063-6294a90a2aae",
                "55b0b7f8-5ac1-f325-e063-6294a90a0b16"
              ],
              "package_ndc": [
                "83566-561-01",
                "87492-002-01",
                "87492-002-02",
                "87492-002-03",
                "87492-002-04",
                "87492-002-05",
                "87655-001-01"
              ],
              "unii": [
                "6SO6U10H04",
                "5965120SH1",
                "515610SU8C",
                "9JS8DS42SV"
              ],
              "nui": [
                "N0000175379",
                "N0000175564"
              ],
              "pharm_class_pe": [
                "Arteriolar Vasodilation [PE]"
              ],
              "pharm_class_epc": [
                "Arteriolar Vasodilator [EPC]"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "PERCOCET                           /00446701/",
            "drugdosagetext": "UNK",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "actiondrug": "6",
            "activesubstance": {
              "activesubstancename": "ACETAMINOPHEN\\OXYCODONE HYDROCHLORIDE\\OXYCODONE TEREPHTHALATE"
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "MULTIVITAMIN",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "actiondrug": "6",
            "activesubstance": {
              "activesubstancename": "VITAMINS"
            },
            "openfda": {
              "brand_name": [
                "LUMAVEX",
                "PNV PRENATOL",
                "INFLAMEX",
                "AFLORA",
                "FOLIXIA",
                "NUTRALYN",
                "FOLCYTEINE",
                "VITALUX",
                "FOLYRA",
                "DAVIMET",
                "DAVIMET-M",
                "FOLATEN",
                "DEXATRAN",
                "FOLARTEX",
                "BOOSTERVITE",
                "MULTIVITAMIN",
                "LUNAVIRA",
                "PRENATOL-M"
              ],
              "generic_name": [
                "MULTIVITAMIN"
              ],
              "manufacturer_name": [
                "Oncora Pharma, LLC",
                "PureTek Corporation"
              ],
              "product_ndc": [
                "85477-610",
                "59088-078",
                "59088-191",
                "85477-904",
                "85477-902",
                "85477-903",
                "59088-795",
                "59088-139",
                "85477-523",
                "59088-695",
                "59088-158",
                "85477-901",
                "59088-643",
                "85477-511",
                "59088-022",
                "59088-018",
                "85477-623",
                "59088-009"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL",
                "CUTANEOUS"
              ],
              "substance_name": [
                "THIAMINE HYDROCHLORIDE",
                "NIACINAMIDE",
                "PYRIDOXINE HYDROCHLORIDE",
                "ASCORBIC ACID",
                "PANTOTHENIC ACID",
                "RIBOFLAVIN",
                "FOLIC ACID",
                "METHYLCOBALAMIN",
                "LEVOMEFOLATE CALCIUM",
                "CYANOCOBALAMIN",
                "CALCIUM CARBONATE",
                "VITAMIN A ACETATE",
                "THIAMINE MONONITRATE",
                "ZINC OXIDE",
                "MANGANESE SULFATE",
                ".ALPHA.-TOCOPHEROL ACETATE, DL-",
                "MAGNESIUM OXIDE",
                "CHROMIUM NICOTINATE",
                "MOLYBDENUM",
                "SELENIUM",
                "CHOLECALCIFEROL",
                "CHOLINE BITARTRATE",
                "FERROUS FUMARATE",
                "POTASSIUM IODIDE",
                "BLACK PEPPER",
                "GARLIC",
                "TURMERIC",
                "FERROUS BISGLYCINATE",
                "BETA CAROTENE",
                "BIOTIN",
                "CALCIUM CITRATE",
                "ACETYLCYSTEINE",
                "MAGNESIUM CITRATE",
                "LEVOMEFOLIC ACID",
                "VITAMIN A",
                "SODIUM ASCORBATE",
                "NIACIN",
                "MAGNESIUM SULFATE HEPTAHYDRATE",
                "CALCIUM PANTOTHENATE",
                "ZINC SULFATE",
                "CUPRIC SULFATE",
                "ORANGE JUICE",
                "BROCCOLI SPROUT",
                "PRUNUS CERASUS (BITTER CHERRY) FRUIT EXTRACT",
                "KALE",
                "WITHANIA SOMNIFERA ROOT"
              ],
              "spl_id": [
                "4139742d-d090-121c-e063-6394a90a6221",
                "583f00c7-1e74-9db6-e063-6294a90a684c",
                "1859a102-9152-018d-e063-6394a90a925f",
                "4aa3dbef-0e2d-49c7-e063-6294a90a9ba9",
                "4aa3e0fa-38cd-3f45-e063-6394a90a9a2b",
                "4aa3f835-f4aa-54bc-e063-6394a90ac250",
                "5592f382-e77e-a812-e063-6294a90a905c",
                "52d5fd35-3a68-5edd-e063-6394a90aba81",
                "d6bfe4ec-21dd-4b6c-8acf-2eda6d409d73",
                "22094f56-c791-2505-e063-6394a90ad0a4",
                "0b67e8de-d81d-0fda-e063-6394a90ac229",
                "4aa443c8-bb31-8f00-e063-6394a90a430d",
                "22078fec-3885-36f9-e063-6294a90aba17",
                "a9886a49-ba1d-44f5-96e5-26c927d6db9c",
                "53efb4bb-24d4-8c55-e063-6394a90ab7b7",
                "353453e2-1f60-24ea-e063-6394a90a251e",
                "474780d5-dd89-8f1a-e063-6294a90a03dc",
                "17559a44-94b8-9ca0-e063-6294a90a2123"
              ],
              "spl_set_id": [
                "4139742d-d091-121c-e063-6394a90a6221",
                "583f0194-0306-f31b-e063-6394a90a2a10",
                "1859a102-9152-018d-e063-6394a90a925f",
                "38e463d1-f608-7cb5-e063-6294a90a4abb",
                "413945b5-116b-d8b6-e063-6394a90a55e8",
                "33da017b-1e8c-d41c-e063-6394a90aab8c",
                "04cf0026-e29b-ffd5-e063-6294a90aca1f",
                "52d5eee7-8146-cc62-e063-6394a90a8c3f",
                "cb182e26-17c5-4d00-869f-08823afeeee8",
                "e4a57710-caa9-51e5-e053-2a95a90a8ad0",
                "0b67e8de-d81e-0fda-e063-6394a90ac229",
                "93086235-2c33-424d-b0c3-213031988581",
                "e052d2c2-7a3f-37be-e053-2a95a90af21c",
                "0a4cb0ab-565f-45e8-a989-740bccef21cd",
                "53efbf65-8844-8486-e063-6394a90a51d3",
                "353453e2-1f60-24ea-e063-6394a90a251e",
                "474780d5-dd88-8f1a-e063-6294a90a03dc",
                "17559a44-94b7-9ca0-e063-6294a90a2123"
              ],
              "package_ndc": [
                "85477-610-30",
                "59088-078-54",
                "59088-191-54",
                "85477-904-30",
                "85477-902-30",
                "85477-903-30",
                "59088-795-54",
                "59088-139-54",
                "85477-523-30",
                "59088-695-54",
                "59088-158-54",
                "85477-901-30",
                "59088-643-54",
                "85477-511-30",
                "59088-022-54",
                "59088-018-54",
                "85477-623-30",
                "59088-009-54"
              ],
              "nui": [
                "N0000193618",
                "M0001797",
                "M0022794",
                "N0000175951",
                "M0022797",
                "N0000175952",
                "N0000185371",
                "N0000175629",
                "N0000184306",
                "M0000728",
                "M0006342",
                "M0022575",
                "M0016962",
                "N0000175429",
                "N0000175961",
                "N0000008867",
                "N0000175960",
                "N0000175776",
                "N0000175547",
                "N0000178369",
                "M0008658",
                "M0022788",
                "N0000175950",
                "N0000175594",
                "M0014839"
              ],
              "pharm_class_epc": [
                "Vitamin C [EPC]",
                "Vitamin B12 [EPC]",
                "Vitamin D [EPC]",
                "Non-Standardized Food Allergenic Extract [EPC]",
                "Antidote [EPC]",
                "Antidote for Acetaminophen Overdose [EPC]",
                "Mucolytic [EPC]",
                "Folate Analog [EPC]",
                "Vitamin A [EPC]",
                "Nicotinic Acid [EPC]"
              ],
              "pharm_class_cs": [
                "Ascorbic Acid [CS]",
                "Vitamin B 12 [CS]",
                "Vitamin D [CS]",
                "Allergens [CS]",
                "Dietary Proteins [CS]",
                "Vegetable Proteins [CS]",
                "Plant Proteins [CS]",
                "Folic Acid [CS]",
                "Vitamin A [CS]",
                "Nicotinic Acids [CS]"
              ],
              "unii": [
                "M572600E5P",
                "25X51I8RD4",
                "68Y4CF58BV",
                "PQ6CK8PD0R",
                "19F5HK2737",
                "TLM2976OFR",
                "935E97BOY8",
                "BR1SN1JS2W",
                "A9R10K3F2F",
                "P6YC3EG204",
                "H0G9379FGK",
                "3LE3D9D6OY",
                "8K0I04919X",
                "SOI2LOH54Z",
                "W00LYS4T26",
                "WR1WPI7EW8",
                "3A3U0GI71G",
                "A150AY412V",
                "81AH48963U",
                "H6241UJ22B",
                "1C6V77QF41",
                "6K2W7T9V6Y",
                "R5L488RY0Q",
                "1C4QK22F9J",
                "KM66971LVF",
                "V1V998DC17",
                "856YO1Z64F",
                "SFW1D987QV",
                "01YAE03M7J",
                "6SO6U10H04",
                "MLM29U2X85",
                "WYQ7N0BPYC",
                "RHO26O1T9V",
                "8S95DH25XC",
                "81G40H8B0T",
                "S033EH8359",
                "2679MF687A",
                "SK47B8698T",
                "568ET80C3D",
                "89DS0H96TB",
                "LRX7AJ16DT",
                "5A9KE2L9L3",
                "128UH9LOAE",
                "1L29G6428X",
                "0Y3L4J38H1",
                "V038D626IF"
              ],
              "pharm_class_pe": [
                "Increased Histamine Release [PE]",
                "Cell-mediated Immunity [PE]",
                "Decreased Respiratory Secretion Viscosity [PE]",
                "Increased Glutathione Concentration [PE]"
              ],
              "pharm_class_moa": [
                "Reduction Activity [MoA]"
              ]
            }
          },
          {
            "drugcharacterization": "1",
            "medicinalproduct": "ZEJULA",
            "drugbatchnumb": "5905798",
            "drugauthorizationnumb": "208447",
            "drugstructuredosagenumb": "200",
            "drugstructuredosageunit": "003",
            "drugdosagetext": "200 MG, QD",
            "drugdosageform": "CAPSULE",
            "drugadministrationroute": "048",
            "actiondrug": "1",
            "activesubstance": {
              "activesubstancename": "NIRAPARIB"
            },
            "openfda": {
              "application_number": [
                "NDA214876"
              ],
              "brand_name": [
                "ZEJULA"
              ],
              "generic_name": [
                "NIRAPARIB"
              ],
              "manufacturer_name": [
                "GlaxoSmithKline LLC"
              ],
              "product_ndc": [
                "0173-0909",
                "0173-0912",
                "0173-0915"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "NIRAPARIB TOSYLATE"
              ],
              "rxcui": [
                "2637449",
                "2637452",
                "2637465",
                "2640210",
                "2640212",
                "2640214"
              ],
              "spl_id": [
                "b5e85656-77f8-405d-982e-c3d890a0f99b"
              ],
              "spl_set_id": [
                "b7f675e2-159c-490c-b6f4-3f16d9492b7d"
              ],
              "package_ndc": [
                "0173-0909-13",
                "0173-0912-13",
                "0173-0912-61",
                "0173-0915-13",
                "0173-0915-61"
              ],
              "unii": [
                "195Q483UZD"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "AMBIEN",
            "drugdosagetext": "UNK",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "actiondrug": "6",
            "activesubstance": {
              "activesubstancename": "ZOLPIDEM TARTRATE"
            },
            "openfda": {
              "application_number": [
                "NDA019908",
                "NDA021774"
              ],
              "brand_name": [
                "AMBIEN",
                "AMBIEN CR"
              ],
              "generic_name": [
                "ZOLPIDEM TARTRATE"
              ],
              "manufacturer_name": [
                "Cosette Pharmaceuticals, Inc.",
                "Sanofi-Aventis U.S. LLC"
              ],
              "product_ndc": [
                "0713-5401",
                "0713-5421",
                "0713-5501",
                "0713-5521",
                "0024-5401",
                "0024-5421"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "ZOLPIDEM TARTRATE"
              ],
              "rxcui": [
                "854873",
                "854875",
                "854876",
                "854878",
                "854880",
                "854882",
                "854894",
                "854896"
              ],
              "spl_id": [
                "2d934208-e709-2948-e063-6294a90aa9b6",
                "2d9350bd-56ea-7273-e063-6394a90a0e61",
                "3d6feaca-4f30-4ca9-a9c8-d9038744fa2f"
              ],
              "spl_set_id": [
                "747949c5-2c91-4909-8a07-71b6826f8e97",
                "2d934da3-bd77-4470-e063-6294a90a64f5",
                "c36cadf4-65a4-4466-b409-c82020b42452"
              ],
              "package_ndc": [
                "0713-5401-01",
                "0713-5421-01",
                "0713-5521-01",
                "0713-5501-01",
                "0024-5401-31",
                "0024-5421-31",
                "0024-5421-50"
              ],
              "unii": [
                "WY6W63843K"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "SYNDROS",
            "drugdosagetext": "UNK",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "actiondrug": "6",
            "activesubstance": {
              "activesubstancename": "DRONABINOL"
            },
            "openfda": {
              "application_number": [
                "NDA205525"
              ],
              "brand_name": [
                "SYNDROS"
              ],
              "generic_name": [
                "DRONABINOL"
              ],
              "manufacturer_name": [
                "Wellhouse Pharma, LLC",
                "Benuvia Operations, LLC"
              ],
              "product_ndc": [
                "85776-201",
                "78613-201"
              ],
              "product_type": [
                "HUMAN PRESCRIPTION DRUG"
              ],
              "route": [
                "ORAL"
              ],
              "substance_name": [
                "DRONABINOL"
              ],
              "rxcui": [
                "1928948",
                "1928954"
              ],
              "spl_id": [
                "dcc02ae3-f1fa-431e-81bb-c52d35b81c66",
                "3e1cbbb1-291c-41bb-b209-93c1fb08313a"
              ],
              "spl_set_id": [
                "3cdcb4f5-5af9-4ff7-b535-2a5cf4c6da89",
                "a7801c70-995d-46a2-91ee-141ef427c6b5"
              ],
              "package_ndc": [
                "85776-201-30",
                "78613-201-30"
              ],
              "nui": [
                "N0000175782",
                "M0003267"
              ],
              "pharm_class_epc": [
                "Cannabinoid [EPC]"
              ],
              "pharm_class_cs": [
                "Cannabinoids [CS]"
              ],
              "unii": [
                "7J8897W37S"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "VITAMIN C",
            "drugdosagetext": "UNK",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "actiondrug": "6",
            "activesubstance": {
              "activesubstancename": "ASCORBIC ACID"
            },
            "openfda": {
              "application_number": [
                "M001"
              ],
              "brand_name": [
                "VITAMIN C SERUM"
              ],
              "generic_name": [
                "VITAMIN C"
              ],
              "manufacturer_name": [
                "FlexiGo Inc"
              ],
              "product_ndc": [
                "85524-2627"
              ],
              "product_type": [
                "HUMAN OTC DRUG"
              ],
              "route": [
                "TOPICAL"
              ],
              "substance_name": [
                "HYALURONIC ACID",
                "NIACINAMIDE",
                "ASCORBIC ACID"
              ],
              "spl_id": [
                "496e7d41-2177-7b0c-e063-6394a90a98f1"
              ],
              "spl_set_id": [
                "496e7d41-2176-7b0c-e063-6394a90a98f1"
              ],
              "package_ndc": [
                "85524-2627-1",
                "85524-2627-2",
                "85524-2627-3",
                "85524-2627-4",
                "85524-2627-5",
                "85524-2627-6"
              ],
              "nui": [
                "N0000193618",
                "M0001797"
              ],
              "pharm_class_epc": [
                "Vitamin C [EPC]"
              ],
              "pharm_class_cs": [
                "Ascorbic Acid [CS]"
              ],
              "unii": [
                "S270N0TRQY",
                "25X51I8RD4",
                "PQ6CK8PD0R"
              ]
            }
          },
          {
            "drugcharacterization": "2",
            "medicinalproduct": "ASTRAGALUS EXTRACT",
            "drugdosagetext": "UNK",
            "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION",
            "actiondrug": "6"
          }
        ]
      }
    }
  ]
}