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
125526871 12552687 1 I 20160417 20160705 20160713 20160713 EXP FR-PFIZER INC-2016340436 PFIZER 67.00 YR M Y 0.00000 20160713 OT FR FR

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
125526871 12552687 1 PS CORDARONE AMIODARONE HYDROCHLORIDE 1 Oral 200 MG, DAILY 18972 200 MG TABLET
125526871 12552687 2 SS KARDEGIC ASPIRIN LYSINE 1 Oral UNK 0 POWDER FOR ORAL SOLUTION
125526871 12552687 3 SS PREVISCAN FLUINDIONE 1 Oral UNK 0 TABLET
125526871 12552687 4 C BISOPROLOL BISOPROLOL 1 UNK 0
125526871 12552687 5 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 UNK 0
125526871 12552687 6 C SOLUPRED PREDNISOLONE 1 UNK 0
125526871 12552687 7 C CRESTOR ROSUVASTATIN CALCIUM 1 UNK 0
125526871 12552687 8 C VIDAZA AZACITIDINE 1 UNK 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125526871 12552687 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125526871 12552687 Gastrointestinal haemorrhage

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
125526871 12552687 1 201603 0
125526871 12552687 3 20160417 0
125526871 12552687 8 20150810 20160415 0