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
126849761 12684976 1 I 20160708 20160818 20160825 20160825 EXP FR-ASTRAZENECA-2016SE89922 ASTRAZENECA 69.00 YR M Y 0.00000 20160825 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
126849761 12684976 1 PS ATACAND CANDESARTAN CILEXETIL 1 Oral 20838 TABLET
126849761 12684976 2 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 0 TABLET
126849761 12684976 3 SS CORDARONE AMIODARONE HYDROCHLORIDE 1 Oral 0
126849761 12684976 4 SS LASILIX FUROSEMIDE 1 Oral 0
126849761 12684976 5 SS ZYLORIC ALLOPURINOL 1 Oral 0
126849761 12684976 6 SS XARELTO RIVAROXABAN 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126849761 12684976 1 Hypertension
126849761 12684976 2 Hyperlipidaemia
126849761 12684976 3 Atrial fibrillation
126849761 12684976 4 Hypertension
126849761 12684976 6 Thrombosis

Outcome of event

Event ID CASEID OUTC COD
126849761 12684976 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126849761 12684976 Vascular purpura

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
126849761 12684976 2 201601 0
126849761 12684976 6 201601 0