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
126439891 12643989 1 I 20160803 20160811 20160811 EXP GB-PFIZER INC-2016373969 PFIZER 70.00 YR M Y 0.00000 20160811 CN GB GB

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
126439891 12643989 1 PS SPIRONOLACTONE. SPIRONOLACTONE 1 Oral 50 MG, UNKNOWN UNKNOWN 12151 50 MG
126439891 12643989 2 SS SPIRONOLACTONE. SPIRONOLACTONE 1 Oral 5 X 40 MG TABLETS (3 AND 2), DAILY UNKNOWN 12151

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126439891 12643989 1 Cardiac failure congestive

Outcome of event

Event ID CASEID OUTC COD
126439891 12643989 OT
126439891 12643989 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126439891 12643989 Cardiac failure
126439891 12643989 Confusional state
126439891 12643989 Decreased appetite
126439891 12643989 Face oedema
126439891 12643989 Incontinence
126439891 12643989 Lower respiratory tract infection
126439891 12643989 Pericardial effusion
126439891 12643989 Renal function test abnormal
126439891 12643989 Urine output decreased

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
126439891 12643989 1 20160524 20160530 0
126439891 12643989 2 20160524 20160528 0