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"da872266-d5f2-35df-096e-341f58d93427" ], "package_ndc": [ "70700-114-85" ] } }, { "drugcharacterization": "2", "medicinalproduct": "NASACORT", "drugseparatedosagenumb": "1", "drugdosagetext": "UNK", "drugdosageform": "Nasal spray", "drugindication": "Product used for unknown indication", "drugstartdateformat": "102", "drugstartdate": "20140218", "drugenddateformat": "102", "drugenddate": "20150519", "drugtreatmentduration": "456", "drugtreatmentdurationunit": "804", "activesubstance": { "activesubstancename": "TRIAMCINOLONE ACETONIDE" }, "openfda": {} }, { "drugcharacterization": "2", "medicinalproduct": "OXYMETAZOLINE", "drugseparatedosagenumb": "1", "drugdosagetext": "UNK", "drugdosageform": "Nasal spray", "drugindication": "Product used for unknown indication", "drugstartdateformat": "102", "drugstartdate": "20070221", "drugenddateformat": "102", "drugenddate": "20150519", "drugtreatmentduration": "3010", "drugtreatmentdurationunit": "804", "activesubstance": { "activesubstancename": "OXYMETAZOLINE" }, "openfda": { "application_number": [ "M012" ], "brand_name": [ "FAMILY WELLNESS OXYMETAZOLINE SINUS SEVERE", "FAMILY WELLNESS OXYMETAZOLINE NO DRIP", "FAMILY WELLNESS OXYMETAZOLINE" ], "generic_name": [ "OXYMETAZOLINE" ], "manufacturer_name": [ "FAMILY DOLLAR (Family Wellness)" ], "product_ndc": [ "55319-827", "55319-983", "55319-985" ], "product_type": [ "HUMAN OTC DRUG" ], "route": [ "NASAL" ], "substance_name": [ "OXYMETAZOLINE HYDROCHLORIDE" ], "rxcui": [ "1000990" ], "spl_id": [ "c2418891-74c7-4963-9ac2-26b745273a6a", "3c853555-c557-4b90-bc8f-277c59c65cbe", "26795e57-311e-4145-9272-4ccbaaa04108" ], "spl_set_id": [ "13237d31-c60a-49f8-9b96-4414cf766a08", "0c006b1c-8ab2-4b9c-8738-e7001c1bb47d", "8b4557d4-74a0-400f-ad7a-6d31473b3c67" ], "package_ndc": [ "55319-827-30", "55319-983-28", "55319-985-28" ], "unii": [ "K89MJ0S5VY" ] } }, { "drugcharacterization": "2", "medicinalproduct": "ZYRTEC", "drugseparatedosagenumb": "1", "drugindication": "Product used for unknown indication", "activesubstance": { "activesubstancename": "CETIRIZINE HYDROCHLORIDE" }, "openfda": { "application_number": [ "NDA021621" ], "brand_name": [ "ZYRTEC" ], "generic_name": [ "CETIRIZINE HYDROCHLORIDE" ], "manufacturer_name": [ "Kenvue Brands LLC" ], "product_ndc": [ "50580-753" ], "product_type": [ "HUMAN OTC DRUG" ], "route": [ "ORAL" ], "substance_name": [ "CETIRIZINE HYDROCHLORIDE" ], "rxcui": [ "1014674", "1020022" ], "spl_id": [ "375f333a-6e53-5140-e063-6294a90a9967" ], "spl_set_id": [ "dc613bd5-70fd-1d9b-e053-2995a90a41cd" ], "package_ndc": [ "50580-753-24" ], "unii": [ "64O047KTOA" ] } }, { "drugcharacterization": "2", "medicinalproduct": "ZEPBOUND", "drugseparatedosagenumb": "1", "drugindication": "Product used for unknown indication", "activesubstance": { "activesubstancename": "TIRZEPATIDE" }, "openfda": { "application_number": [ "NDA217806" ], "brand_name": [ "ZEPBOUND", "ZEPBOUND KWIKPEN" ], "generic_name": [ "TIRZEPATIDE" ], "manufacturer_name": [ "Eli Lilly and Company" ], "product_ndc": [ "0002-0152", "0002-2506", "0002-2495", "0002-2484", "0002-2471", "0002-2460", "0002-2457", "0002-0243", "0002-1214", "0002-1340", "0002-1423", "0002-2002", "0002-6052", "0002-6103", "0002-6210", "0002-6304", "0002-6523", "0002-6612", "0002-3566", "0002-3555", "0002-3544", "0002-3533", "0002-3522", "0002-3511" ], "product_type": [ "HUMAN PRESCRIPTION DRUG" ], "route": [ "SUBCUTANEOUS" ], "substance_name": [ "TIRZEPATIDE" ], "rxcui": [ "2601743", "2601755", "2601761", "2601767", "2601773", "2601784", "2644396", "2644401", "2644405", "2644409", "2644413", "2644417", "2669706", "2669709", "2669712", "2669715", "2669718", "2669721", "2679317", "2679319", "2679321", "2679323", "2679325", "2679327", "2732437", "2732440", "2732442", "2732444", "2732446", "2732448", "2732449", "2732450", "2732452", "2732454", "2732456", "2732458", "2734623", "2734626", "2734628", "2734630", "2734632", "2734634", "2734636", "2734638", "2734640", "2734642", "2734644", "2734646" ], "spl_id": [ "f4a0acea-cd2f-4e90-b495-bb07116e0509" ], "spl_set_id": [ "487cd7e7-434c-4925-99fa-aa80b1cc776b" ], "package_ndc": [ "0002-2506-01", "0002-2506-80", "0002-2506-61", "0002-2495-01", "0002-2495-80", "0002-2484-01", "0002-2484-80", "0002-2471-01", "0002-2471-80", "0002-2460-01", "0002-2460-80", "0002-2457-01", "0002-2457-80", "0002-0152-01", "0002-0152-04", "0002-0152-61", "0002-0243-01", "0002-0243-04", "0002-1214-01", "0002-1214-04", "0002-1340-01", "0002-1340-04", "0002-1423-01", "0002-1423-04", "0002-2002-01", "0002-2002-04", "0002-6052-01", "0002-6052-11", "0002-6103-01", "0002-6103-11", "0002-6210-01", "0002-6210-11", "0002-6304-01", "0002-6304-11", "0002-6523-01", "0002-6523-11", "0002-6612-01", "0002-6612-11", "0002-3566-01", "0002-3566-11", "0002-3566-99", "0002-3555-01", "0002-3555-11", "0002-3544-01", "0002-3544-11", "0002-3533-01", "0002-3533-11", "0002-3522-01", "0002-3522-11", "0002-3511-01", "0002-3511-11" ], "nui": [ "N0000194015", "N0000000152", "N0000178480", "N0000020058" ], "pharm_class_epc": [ "Glucose-dependent Insulinotropic Polypeptide Receptor Agonist [EPC]", "GLP-1 Receptor Agonist [EPC]" ], "pharm_class_moa": [ "G-Protein-linked Receptor Interactions [MoA]", "Glucagon-like Peptide-1 (GLP-1) Agonists [MoA]" ], "unii": [ "OYN3CCI6QE" ] } } ], "summary": { "narrativeincludeclinical": "CASE EVENT DATE: 20140310" } } } ] }