The Safety Rates Drug Report

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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
125840161 12584016 1 I 20160713 20160722 20160722 EXP GB-MHRA-MIDB-4042EED3-8141-4481-A70C-AC7D7E5B7A11 GB-MYLANLABS-2016M1029265 MYLAN 0.00 Y 0.00000 20160722 PH 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
125840161 12584016 1 PS LISINOPRIL. LISINOPRIL 1 5 MG, QD Y U 76071 5 MG QD
125840161 12584016 2 SS WARFARIN WARFARIN 1 1 MG, UNK Y U 0 1 MG
125840161 12584016 3 C FUROSEMIDE. FUROSEMIDE 1 40 MG, QD (IN THE MORNING) U 0 40 MG QD
125840161 12584016 4 C OMEPRAZOLE. OMEPRAZOLE 1 20 MG, QD (IN THE MORNING) U 0 20 MG QD
125840161 12584016 5 C SIMVASTATIN. SIMVASTATIN 1 20 MG, QD (AT NIGHT) U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125840161 12584016 2 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125840161 12584016 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125840161 12584016 Bradycardia
125840161 12584016 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
125840161 12584016 1 20160511 0
125840161 12584016 2 20160511 0