{ "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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"42385-979-72", "42385-980-30", "42385-980-90", "42385-980-01", "42385-980-05", "42385-980-11", "42385-980-72", "65162-698-90", "65162-698-39", "65162-698-54", "64380-753-01", "64380-753-02", "64380-753-03", "64380-754-01", "64380-754-02", "64380-754-03", "64380-731-01", "64380-731-02", "64380-731-03" ], "nui": [ "N0000008486" ], "pharm_class_pe": [ "Decreased Central Nervous System Disorganized Electrical Activity [PE]" ], "unii": [ "6CW7F3G59X" ] } }, { "drugcharacterization": "1", "medicinalproduct": "CIPROFLOXACIN HCL", "drugseparatedosagenumb": "2", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "804", "drugdosagetext": "? QUANTITY:1 TABLET(S);?", "drugdosageform": "COATED TABLET", "drugadministrationroute": "048", "drugindication": "INFECTION PROPHYLAXIS", "drugstartdateformat": "102", "drugstartdate": "20100821", "drugenddateformat": "102", "drugenddate": "20190822", "drugadditional": "2", "activesubstance": { "activesubstancename": "CIPROFLOXACIN HYDROCHLORIDE" }, "openfda": {} }, { "drugcharacterization": "2", "medicinalproduct": "AMANTADINE.", "activesubstance": { "activesubstancename": "AMANTADINE HYDROCHLORIDE" }, "openfda": { "application_number": [ "NDA208944", "ANDA075060", "ANDA214284", "ANDA208966" ], "brand_name": [ "GOCOVRI", "AMANTADINE" ], "generic_name": [ "AMANTADINE" ], "manufacturer_name": [ "Adamas Pharma, LLC", "AvPAK", "Alembic Pharmaceuticals Limited", "Alembic Pharmaceuticals Inc.", "Supernus Pharmaceuticals", "Xttrium Laboratories, Inc" ], "product_ndc": [ "70482-085", "70482-170", "50268-036", "46708-586", "62332-586", "62332-246", "17772-085", "17772-170", "46708-246", "0116-4010" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "ORAL" ], "substance_name": [ "AMANTADINE", "AMANTADINE HYDROCHLORIDE" ], "rxcui": [ "1944370", "1944376", "1944380", "1944382", "849385", "849395", "849389" ], "spl_id": [ "41c15d67-44b5-5c87-e063-6294a90adcc8", "48c949ef-d92b-abba-e063-6394a90a2d2a", "1ca812f6-6983-4d9a-b08e-a8f7e50054b8", "a9507ffa-0c95-48ce-80bf-60bc699add17", "416dbd88-4408-43c2-b47d-c14911c050d0", "4af3ee09-faf9-9840-e063-6394a90aafdc", "db464488-fe29-445d-b8c1-b93554371798", "3479947d-22a8-67e8-e063-6294a90ae41c" ], "spl_set_id": [ "82ff865f-78f3-4c94-b6a9-727a54944b28", "48c949e3-86e0-c639-e063-6294a90acdba", "48fa07c8-8b95-40d7-a0f5-132577dfb2c8", "da1837b5-fda2-48e0-91ba-d6eb2b991b55", "4157d9a7-a53f-4dde-b051-fe3e9a674913", "2bee0631-0028-1314-e063-6394a90aaaed", "d8887814-3e56-447e-8bc3-add1861e0cf7", "25dd8a3c-6b11-2ea1-e063-6294a90a50cf" ], "package_ndc": [ "70482-085-60", "70482-085-21", "70482-085-61", "70482-170-60", "70482-170-21", "70482-170-61", "50268-036-11", "50268-036-14", "46708-586-31", "46708-586-71", "62332-586-31", "62332-586-71", "62332-246-30", "62332-246-31", "62332-246-71", "62332-246-91", "17772-085-60", "17772-085-21", "17772-170-60", "17772-170-21", "46708-246-30", "46708-246-31", "46708-246-71", "46708-246-91", "0116-4010-16", "0116-4010-10", "0116-4010-41" ], "nui": [ "N0000175543", "N0000175542" ], "pharm_class_epc": [ "Influenza A M2 Protein Inhibitor [EPC]" ], "pharm_class_moa": [ "M2 Protein Inhibitors [MoA]" ], "unii": [ "BF4C9Z1J53", "M6Q1EO9TD0" ] } }, { "drugcharacterization": "2", "medicinalproduct": "MELATONIN", "activesubstance": { "activesubstancename": "MELATONIN" }, "openfda": { "brand_name": [ "MELATONIN", "MELATONIN PHENOLIC", "MELATONIN CORD", "MELATONIN 1527" ], "generic_name": [ "MELATONIN" ], "manufacturer_name": [ "BioActive Nutritional, Inc.", "Energique, Inc.", "Professional Complementary Health Formulas", "Deseret Biologicals, Inc." ], "product_ndc": [ "43857-0511", "43857-0086", "44911-0247", "44911-0194", "63083-1527", "43742-0771" ], "product_type": [ "HUMAN OTC DRUG" ], "route": [ "ORAL" ], "substance_name": [ "MELATONIN" ], "spl_id": [ "adcac0e0-d21f-4124-b951-e6913591ac9f", "e189499d-9da3-43fc-8a0b-9d5dd0923b11", "adde04ad-3287-4fe9-b9e5-6385123b7da3", "3c4502c5-e02b-43e1-94e8-55f92983e63c", "149c1dc0-8f8d-4b51-9caa-c74ed9c86822", "43f1b593-3e12-4009-af39-7d4b35a291ea" ], "spl_set_id": [ "8951e5e9-5d8f-4808-b247-208760fae656", "cd82eb5d-a44a-4512-ad65-0fffae70d1d0", "895cb8a5-33ea-4764-86a6-1da513dcd2c1", "9a59554b-14c4-4c79-9db1-0a38b3c152f2", "eb411c99-fe69-400d-b452-95d8d6d754b8", "4ea9b3dc-a6f7-48b0-b0a7-ac2951bc575d" ], "package_ndc": [ "43857-0511-1", "43857-0086-1", "44911-0247-1", "44911-0194-1", "63083-1527-1", "43742-0771-1" ], "unii": [ "JL5DK93RCL" ] } }, { "drugcharacterization": "2", "medicinalproduct": "CARBIDOPA/LEVODOPA", "activesubstance": { "activesubstancename": "CARBIDOPA\\LEVODOPA" } }, { "drugcharacterization": "2", "medicinalproduct": "VITAMIN C", "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" ] } } ], "summary": { "narrativeincludeclinical": "CASE EVENT DATE: 20190822" } } } ] }