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
127747761 12774776 1 I 20150502 20160919 20160923 20160923 EXP ES-AGEMED-842765340 ES-PFIZER INC-2016440969 PFIZER 78.00 YR M Y 0.00000 20160923 MD ES ES

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
127747761 12774776 1 PS ALDACTONE SPIRONOLACTONE 1 Oral Y 12151 FILM-COATED TABLET
127747761 12774776 2 I COTRIMOXAZOL SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral Y 0
127747761 12774776 3 I ENALAPRIL ENALAPRIL 1 Oral Y 0
127747761 12774776 4 C FUROSEMIDE. FUROSEMIDE 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127747761 12774776 1 Hepatic cirrhosis
127747761 12774776 2 Listeriosis
127747761 12774776 3 Hypertension
127747761 12774776 4 Hepatic cirrhosis

Outcome of event

Event ID CASEID OUTC COD
127747761 12774776 HO
127747761 12774776 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127747761 12774776 Acute kidney injury
127747761 12774776 Drug interaction
127747761 12774776 Hyperkalaemia

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
127747761 12774776 1 201001 20150505 0
127747761 12774776 2 20150428 20150505 0
127747761 12774776 3 20150505 0
127747761 12774776 4 201211 20150505 0