The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
111601232 11160123 2 F 20160728 20150603 20160802 PER US-PFIZER INC-2015188151 PFIZER 74.00 YR F Y 0.00000 20160802 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
111601232 11160123 1 PS LYRICA PREGABALIN 1 UNK U 21446
111601232 11160123 2 SS PROCARDIA NIFEDIPINE 1 UNK U 18482 CAPSULE, SOFT
111601232 11160123 3 SS PLAVIX CLOPIDOGREL BISULFATE 1 UNK U 0
111601232 11160123 4 SS LOTRIL ENALAPRIL MALEATE 1 UNK U 0
111601232 11160123 5 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 UNK U 0
111601232 11160123 6 SS DIGOXIN. DIGOXIN 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
111601232 11160123 Drug hypersensitivity

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found