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
126439871 12643987 1 I 20150729 20160811 20160811 EXP JP-PFIZER INC-2015256660 PFIZER 82.00 YR M Y 0.00000 20160811 MD JP JP

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
126439871 12643987 1 PS SPIRONOLACTONE. SPIRONOLACTONE 1 25 MG, DAILY Y 12151 25 MG TABLET

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126439871 12643987 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126439871 12643987 Gynaecomastia
126439871 12643987 Pneumonia

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

no results found

Therapies reported

no results found