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
126965822 12696582 2 F 2016 20160830 20160830 20160906 EXP US-PFIZER INC-2016400363 PFIZER 54.00 YR M Y 0.00000 20160906 CN 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
126965822 12696582 1 PS VIAGRA SILDENAFIL CITRATE 1 100MG TABLETS 20895 FILM-COATED TABLET
126965822 12696582 2 C COUMADIN WARFARIN SODIUM 1 4 MG, 1X/DAY 0 4 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126965822 12696582 1 Cardiovascular disorder
126965822 12696582 2 Anticoagulant therapy

Outcome of event

Event ID CASEID OUTC COD
126965822 12696582 HO
126965822 12696582 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126965822 12696582 Abdominal distension
126965822 12696582 Asthenia
126965822 12696582 Condition aggravated
126965822 12696582 Crohn's disease
126965822 12696582 Dyspnoea
126965822 12696582 Fluid retention
126965822 12696582 Haematochezia
126965822 12696582 Peripheral swelling
126965822 12696582 Product use issue
126965822 12696582 Pulmonary thrombosis
126965822 12696582 Renal failure
126965822 12696582 Weight increased

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

no results found

Therapies reported

no results found