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
113134883 11313488 3 F 20160715 20150727 20160725 EXP US-PFIZER INC-2015245133 PFIZER 0.00 F Y 0.00000 20160725 CN 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
113134883 11313488 1 PS ALDACTONE SPIRONOLACTONE 1 UNK U 12151 TABLET
113134883 11313488 2 SS VERAPAMIL HCL VERAPAMIL HYDROCHLORIDE 1 UNK U 18817
113134883 11313488 3 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 UNK U 74133
113134883 11313488 4 SS ERYTHROMYCIN. ERYTHROMYCIN 1 UNK U 50609
113134883 11313488 5 SS COREG CARVEDILOL 1 UNK U 0
113134883 11313488 6 SS LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113134883 11313488 1 Hypertension
113134883 11313488 2 Hypertension
113134883 11313488 3 Hypertension
113134883 11313488 4 Product used for unknown indication
113134883 11313488 5 Hypertension
113134883 11313488 6 Hypertension

Outcome of event

Event ID CASEID OUTC COD
113134883 11313488 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113134883 11313488 Anaphylactic reaction

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

no results found

Therapies reported

no results found