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
87158893 8715889 3 F 20121002 20120725 20121010 EXP AUR-APL-2012-03171 AUROBINDO 72.00 YR F N 0.00000 20121009 OT DK

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
87158893 8715889 1 PS METFORMIN 1 D 77095 2 GM QD
87158893 8715889 2 C DIGOXIN (DIGOXIN) 1 0
87158893 8715889 3 C WARFARIN SODIUM 1 0
87158893 8715889 4 C SIMVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
87158893 8715889 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
87158893 8715889 OT
87158893 8715889 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
87158893 8715889 Abdominal pain
87158893 8715889 Alanine aminotransferase increased
87158893 8715889 Amylase increased
87158893 8715889 Anuria
87158893 8715889 Blood creatine phosphokinase MB increased
87158893 8715889 Blood glucose increased
87158893 8715889 Chest pain
87158893 8715889 Dehydration
87158893 8715889 Dyspnoea
87158893 8715889 Haemodialysis
87158893 8715889 Lactic acidosis
87158893 8715889 Renal impairment
87158893 8715889 Sepsis
87158893 8715889 Troponin I increased
87158893 8715889 White blood cell count increased

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

Event ID CASEID RPSR COD
87158893 8715889 FGN
87158893 8715889 HP
87158893 8715889 LIT

Therapies reported

no results found