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
127895491 12789549 1 I 20160920 20160928 20160928 EXP US-PFIZER INC-2016442440 PFIZER 66.00 YR F Y 74.00000 KG 20160928 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
127895491 12789549 1 PS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 50 MG, 2X/DAY U 74133 50 MG BID
127895491 12789549 2 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 100 MG, 1X/DAY U 74133 100 MG QD
127895491 12789549 3 SS HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 25 MG, DAILY N 0 25 MG
127895491 12789549 4 SS LISINOPRIL. LISINOPRIL 1 20 MG, 1X/DAY U 0 20 MG QD
127895491 12789549 5 C ATORVASTATIN ATORVASTATIN 1 0
127895491 12789549 6 C ASPIRIN. ASPIRIN 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127895491 12789549 OT
127895491 12789549 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127895491 12789549 Amyloidosis
127895491 12789549 Atrial fibrillation
127895491 12789549 Cardiac amyloidosis
127895491 12789549 Cardiac failure
127895491 12789549 Disease progression
127895491 12789549 General physical health deterioration

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127895491 12789549 2 20150715 0