Name: FDA Drug Adverse Events
Creator: ModernRelay

Mmodernrelayfda-drug-adverse-events

FDA Drug Adverse Events

Reported side effects and adverse reactions to drugs after they reach the market (FDA FAERS), including patient details, the suspected drugs, reported reactions, and patient outcomes such as hospitalization or death

Adverse Event Drugs Data

Adverse Event Drugs records
Drug Key	Action Taken	Active Substance	Administration Route	Authorization Number	Dosage Text	Drug Role	Indication	Medicinal Product
10004820:0	5	PHENYTOIN	048	84349	100 MG, 2X/DAY	1	EPILEPSY	DILANTIN
10004820:1	5	PHENYTOIN		84349	200 MG, 2X/DAY	1	PARTIAL SEIZURES	DILANTIN
10004823:0	5	ATORVASTATIN CALCIUM	048	020702	UNK	1	LOW DENSITY LIPOPROTEIN INCREASED	LIPITOR
10004823:1	5	ATORVASTATIN CALCIUM

	Drug Key	Report	Safety Report ID	Action Taken	Active Substance	Administration Route	Authorization Number	Dosage Text	Drug Role	Drug Start Date	Indication	Medicinal Product	OpenFDA Application Numbers	OpenFDA Brand Names	OpenFDA Generic Names	OpenFDA Manufacturer Names	OpenFDA Pharmacologic Class (EPC)	OpenFDA Pharmacologic Class (MOA)	OpenFDA RxCUI	OpenFDA SPL Set ID	OpenFDA Substance Names	OpenFDA UNII

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