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
126555371 12655537 1 I 20160630 20160811 20160816 20160816 EXP FR-ASTRAZENECA-2016SE87383 ASTRAZENECA 30915.00 DY F Y 0.00000 20160816 MD 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
126555371 12655537 1 PS ATACAND CANDESARTAN CILEXETIL 1 Oral Y 20838 4 MG TABLET QD
126555371 12655537 2 SS LASILIX SPECIAL FUROSEMIDE 1 Oral Y 0 125 MG QD
126555371 12655537 3 SS LASILIX SPECIAL FUROSEMIDE 1 Oral Y 0
126555371 12655537 4 C COUMADINE WARFARIN SODIUM 1 Oral 0
126555371 12655537 5 C ATORVASTATINE ATORVASTATIN 1 0
126555371 12655537 6 C BISOPROLOL BISOPROLOL 1 0
126555371 12655537 7 C LANTUS INSULIN GLARGINE 1 0
126555371 12655537 8 C BRICANYL TERBUTALINE SULFATE 1 0
126555371 12655537 9 C ATROVENT IPRATROPIUM BROMIDE 1 0
126555371 12655537 10 C AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126555371 12655537 10 Thrombophlebitis septic

Outcome of event

Event ID CASEID OUTC COD
126555371 12655537 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126555371 12655537 Acute kidney injury

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
126555371 12655537 1 20160630 0
126555371 12655537 4 20160630 0
126555371 12655537 10 20160704 0