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
126573571 12657357 1 I 20160712 20160808 20160816 20160816 EXP US-SA-2016SA146440 AVENTIS 69.00 YR E F Y 0.00000 20160816 OT 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
126573571 12657357 1 SS FUROSEMIDE. FUROSEMIDE 1 Unknown Y UNKNOWN 0
126573571 12657357 2 PS IRBESARTAN. IRBESARTAN 1 Unknown Y UNKNOWN 20757
126573571 12657357 3 C ATORVASTATIN ATORVASTATIN 1 Unknown 0
126573571 12657357 4 C NICORANDIL NICORANDIL 1 Unknown 0
126573571 12657357 5 C DILTIAZEM. DILTIAZEM 1 Unknown 0
126573571 12657357 6 C GABAPENTIN. GABAPENTIN 1 Unknown 0
126573571 12657357 7 C SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown 0
126573571 12657357 8 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown 0
126573571 12657357 9 C FLUTICASONE FLUTICASONEFLUTICASONE PROPIONATE 1 Unknown 0
126573571 12657357 10 C ZAPAIN ACETAMINOPHENCODEINE PHOSPHATE 1 Unknown 0
126573571 12657357 11 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Unknown 0
126573571 12657357 12 C AMITRIPTYLINE AMITRIPTYLINE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126573571 12657357 1 Cardiovascular disorder

Outcome of event

Event ID CASEID OUTC COD
126573571 12657357 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126573571 12657357 Hyperkalaemia

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
126573571 12657357 1 20160712 0
126573571 12657357 2 20160712 0