{ "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. 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"76045-010", "76045-121", "42858-122", "42858-234", "42858-338", "42858-416" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS", "ORAL" ], "substance_name": [ "HYDROMORPHONE HYDROCHLORIDE" ], "rxcui": [ "897756", "897757", "1433251", "1872265", "1872269", "1872752", "2277368", "2277370", "897657", "897658", "897696", "897698", "897702", "897704", "897710", "897712" ], "spl_id": [ "002d5650-24df-4b60-a5ce-e7adc091026f", "3348b431-907c-4f1d-8a18-e4be2a04df23" ], "spl_set_id": [ "9eebd88a-5632-460f-b7b6-26c8a180540d", "d6b40e39-a57e-402c-b4f6-7041e832f837" ], "package_ndc": [ "76045-009-96", "76045-009-06", "76045-009-01", "76045-009-11", "76045-010-01", "76045-010-11", "76045-121-01", "76045-121-11", "42858-122-01", "42858-234-01", "42858-234-50", "42858-338-01", "42858-416-16" ], "unii": [ "L960UP2KRW" ] } }, { "drugcharacterization": "2", "medicinalproduct": "DILAUDID", "drugdosageform": "FORMULATION UNKNOWN", "drugindication": "OESOPHAGITIS", "activesubstance": { "activesubstancename": "HYDROMORPHONE HYDROCHLORIDE" }, "openfda": { "application_number": [ "NDA019034", "NDA019892", "NDA019891" ], "brand_name": [ "DILAUDID" ], "generic_name": [ "HYDROMORPHONE HYDROCHLORIDE" ], "manufacturer_name": [ "Fresenius Kabi USA, LLC", "Rhodes Pharmaceuticals LLC" ], "product_ndc": [ "76045-009", "76045-010", "76045-121", "42858-122", "42858-234", "42858-338", "42858-416" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS", "ORAL" ], "substance_name": [ "HYDROMORPHONE HYDROCHLORIDE" ], "rxcui": [ "897756", "897757", "1433251", "1872265", "1872269", "1872752", "2277368", "2277370", "897657", "897658", "897696", "897698", "897702", "897704", "897710", "897712" ], "spl_id": [ "002d5650-24df-4b60-a5ce-e7adc091026f", "3348b431-907c-4f1d-8a18-e4be2a04df23" ], "spl_set_id": [ "9eebd88a-5632-460f-b7b6-26c8a180540d", "d6b40e39-a57e-402c-b4f6-7041e832f837" ], "package_ndc": [ "76045-009-96", "76045-009-06", "76045-009-01", "76045-009-11", "76045-010-01", "76045-010-11", "76045-121-01", "76045-121-11", "42858-122-01", "42858-234-01", "42858-234-50", "42858-338-01", "42858-416-16" ], "unii": [ "L960UP2KRW" ] } }, { "drugcharacterization": "2", "medicinalproduct": "AZITHROMYCIN ANHYDROUS.", "drugstructuredosagenumb": "500", "drugstructuredosageunit": "003", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "804", "drugdosageform": "FORMULATION UNKNOWN", "drugadministrationroute": "042", "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION", "actiondrug": "5", "drugadditional": "3", "activesubstance": { "activesubstancename": "AZITHROMYCIN ANHYDROUS" } }, { "drugcharacterization": "2", "medicinalproduct": "SOLU-MEDROL", "drugstructuredosagenumb": "50", "drugstructuredosageunit": "003", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "804", "drugdosageform": "FORMULATION UNKNOWN", "drugadministrationroute": "042", "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION", "actiondrug": "5", "drugadditional": "3", "activesubstance": { "activesubstancename": "METHYLPREDNISOLONE SODIUM SUCCINATE" }, "openfda": { "application_number": [ "NDA011856" ], "brand_name": [ "SOLU-MEDROL" ], "generic_name": [ "METHYLPREDNISOLONE SODIUM SUCCINATE" ], "manufacturer_name": [ "Pharmacia & Upjohn Company LLC" ], "product_ndc": [ "0009-0003", "0009-0758", "0009-0698", "0009-0039", "0009-0047", "0009-0018", "0009-0850" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "INTRAMUSCULAR", "INTRAVENOUS" ], "substance_name": [ "METHYLPREDNISOLONE SODIUM SUCCINATE" ], "rxcui": [ "207191", "207193", "311659", "314099", "1357886", "1357888", "1743704", "1743707", "1743720", "1743722", "1743726", "1743729" ], "spl_id": [ "c157d266-8633-4c2e-ae1f-0207e4f19b35", "9fdbd924-74fd-4b07-882c-d7e11b1a4642" ], "spl_set_id": [ "cd99be87-c8d9-48d6-a8e5-e081052e3f19", "7271310c-7764-4812-aa30-a5e90987c7a9" ], "package_ndc": [ "0009-0758-01", "0009-0698-01", "0009-0039-30", "0009-0039-28", "0009-0039-33", "0009-0039-32", "0009-0047-25", "0009-0047-22", "0009-0047-27", "0009-0047-26", "0009-0003-02", "0009-0018-20", "0009-0850-01", "0009-0698-02", "0009-0039-05", "0009-0039-06", "0009-0047-03", "0009-0047-04" ], "unii": [ "LEC9GKY20K" ] } }, { "drugcharacterization": "2", "medicinalproduct": "ZOFRAN", "drugstructuredosagenumb": "4", "drugstructuredosageunit": "003", "drugdosageform": "FORMULATION UNKNOWN", "drugadministrationroute": "040", "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION", "actiondrug": "5", "drugadditional": "3", "activesubstance": { "activesubstancename": "ONDANSETRON HYDROCHLORIDE" } }, { "drugcharacterization": "2", "medicinalproduct": "PROTONIX", "drugstructuredosagenumb": "40", "drugstructuredosageunit": "003", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "12", "drugintervaldosagedefinition": "805", "drugdosageform": "FORMULATION UNKNOWN", "drugadministrationroute": "042", "drugindication": "PRODUCT USED FOR UNKNOWN INDICATION", "actiondrug": "5", "drugadditional": "3", "activesubstance": { "activesubstancename": "PANTOPRAZOLE SODIUM" }, "openfda": { "application_number": [ "NDA020988", "NDA020987", "NDA022020" ], "brand_name": [ "PROTONIX I.V.", "PROTONIX DELAYED-RELEASE" ], "generic_name": [ "PANTOPRAZOLE SODIUM" ], "manufacturer_name": [ "Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc." ], "product_ndc": [ "0008-0923", "0008-4001", "0008-0841", "0008-0843", "0008-0844" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "INTRAVENOUS", "ORAL" ], "substance_name": [ "PANTOPRAZOLE SODIUM" ], "rxcui": [ "283669", "885257", "251872", "284400", "314200", "352125", "763306", "763308" ], "spl_id": [ "a7e7d657-a748-4234-8dd6-c0e4d0f81a86", "d36cd2fb-517f-44e5-8438-53e563775f86", "b1adaee5-9353-48ce-bde4-f169a3787e30" ], "spl_set_id": [ "51e4144a-489e-436c-609a-39305f8f56ba", "f39b3e7d-39d2-4c8a-9974-4ab885241880", "08098cb2-c048-4640-f387-6beec4a38936" ], "package_ndc": [ "0008-0923-51", "0008-0923-60", "0008-0923-55", "0008-4001-01", "0008-4001-10", "0008-4001-25", "0008-0843-81", "0008-0841-81", "0008-0844-01", "0008-0844-02" ], "unii": [ "6871619Q5X" ] } } ], "summary": { "narrativeincludeclinical": "CASE EVENT DATE: 20180805" } } } ] }