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[ "HUMAN PRESCRIPTION DRUG" ], "route": [ "INTRAMUSCULAR" ], "substance_name": [ "EPINEPHRINE" ], "rxcui": [ "727316", "727347", "727386", "1870207" ], "spl_id": [ "81569d26-e9b3-4c1d-ac34-8a4cf5b4a98b" ], "spl_set_id": [ "7560c201-9246-487c-a13b-6295db04274a" ], "package_ndc": [ "49502-500-01", "49502-500-02", "49502-500-92", "49502-501-01", "49502-501-02", "49502-501-92" ], "nui": [ "N0000000209", "N0000000245", "N0000175552", "N0000175555", "N0000175570", "M0003647" ], "pharm_class_moa": [ "Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]" ], "pharm_class_epc": [ "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]", "Catecholamine [EPC]" ], "pharm_class_cs": [ "Catecholamines [CS]" ], "unii": [ "YKH834O4BH" ] } }, { "drugcharacterization": "2", "medicinalproduct": "ATROVENT", "drugbatchnumb": "UNKNOWN", "drugdosagetext": "UNK", "drugindication": "Product used for unknown indication", "activesubstance": { "activesubstancename": "IPRATROPIUM BROMIDE" }, "openfda": { "application_number": [ "NDA021527" ], "brand_name": [ "ATROVENT HFA" ], "generic_name": [ "IPRATROPIUM BROMIDE" ], "manufacturer_name": [ "Boehringer Ingelheim Pharmaceuticals, Inc." ], "product_ndc": [ "0597-0087" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "RESPIRATORY (INHALATION)" ], "substance_name": [ "IPRATROPIUM BROMIDE" ], "rxcui": [ "836343", "836368" ], "spl_id": [ "73904f10-4e08-4277-adf6-b605468eb05e" ], "spl_set_id": [ "170e98ef-5560-4068-be7d-e649068eb884" ], "package_ndc": [ "0597-0087-17" ], "unii": [ "J697UZ2A9J" ] } }, { "drugcharacterization": "2", "medicinalproduct": "SPIRIVA", "drugbatchnumb": "UNKNOWN", "drugstructuredosagenumb": "2", "drugstructuredosageunit": "032", "drugseparatedosagenumb": "1", "drugintervaldosageunitnumb": "1", "drugintervaldosagedefinition": "804", "drugdosagetext": "2 DOSAGE FORM, QD", "drugindication": "Product used for unknown indication", "drugstartdateformat": "610", "drugstartdate": "202302", "activesubstance": { "activesubstancename": "TIOTROPIUM BROMIDE MONOHYDRATE" }, "openfda": { "application_number": [ "NDA021395" ], "brand_name": [ "SPIRIVA HANDIHALER" ], "generic_name": [ "TIOTROPIUM BROMIDE" ], "manufacturer_name": [ "Boehringer Ingelheim Pharmaceuticals, Inc." ], "product_ndc": [ "0597-0075" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "ORAL", "RESPIRATORY (INHALATION)" ], "substance_name": [ "TIOTROPIUM BROMIDE MONOHYDRATE" ], "rxcui": [ "485032", "580261" ], "spl_id": [ "94768574-0d3e-46f0-9f75-ab3c9f52857d" ], "spl_set_id": [ "820839ef-e53d-47e8-a3b9-d911ff92e6a9" ], "package_ndc": [ "0597-0075-41", "0597-0075-75", "0597-0075-47" ], "unii": [ "L64SXO195N" ] } }, { "drugcharacterization": "2", "medicinalproduct": "COMBIVENT", "drugbatchnumb": "UNKNOWN", "drugdosagetext": "UNK", "drugindication": "Product used for unknown indication", "activesubstance": { "activesubstancename": "ALBUTEROL SULFATE\\IPRATROPIUM BROMIDE" } }, { "drugcharacterization": "2", "medicinalproduct": "BILASTINE", "drugbatchnumb": "UNKNOWN", "drugindication": "Product used for unknown indication", "activesubstance": { "activesubstancename": "BILASTINE" } } ], "summary": { "narrativeincludeclinical": "CASE EVENT DATE: 20120821" } } } ] }