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
127199541 12719954 1 I 20160404 0 20160906 20160906 DIR FDA-CTU 70.00 YR M N 77.60000 KG 20160617 N PH 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
127199541 12719954 1 PS LISINOPRIL. LISINOPRIL 1 Oral Y D 0 10 MG QD
127199541 12719954 2 SS SPIRONOLACTONE. SPIRONOLACTONE 1 Oral Y D 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127199541 12719954 1 Hypertension
127199541 12719954 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127199541 12719954 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127199541 12719954 Acute kidney injury
127199541 12719954 Bronchitis
127199541 12719954 Cough
127199541 12719954 Dehydration
127199541 12719954 Hyperkalaemia
127199541 12719954 Pain in extremity
127199541 12719954 Pancytopenia

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

Event ID CASEID RPSR COD
127199541 12719954 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127199541 12719954 1 20160226 20160404 0
127199541 12719954 2 20160227 20160404 0