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
126935871 12693587 1 I 20160708 20160818 20160829 20160829 EXP FR-PFIZER INC-2016403136 PFIZER 69.00 YR M Y 0.00000 20160829 OT 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
126935871 12693587 1 PS CORDARONE AMIODARONE HYDROCHLORIDE 1 Oral UNK 18972 TABLET
126935871 12693587 2 SS LASILIX FUROSEMIDE 1 Oral UNK 0
126935871 12693587 3 SS ZYLORIC ALLOPURINOL 1 Oral UNK 0
126935871 12693587 4 SS ATACAND CANDESARTAN CILEXETIL 1 Oral UNK 0
126935871 12693587 5 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral UNK 0
126935871 12693587 6 SS XARELTO RIVAROXABAN 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126935871 12693587 1 Atrial fibrillation
126935871 12693587 2 Hypertension
126935871 12693587 4 Hypertension
126935871 12693587 5 Hyperlipidaemia
126935871 12693587 6 Thrombosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126935871 12693587 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126935871 12693587 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
126935871 12693587 5 201601 0
126935871 12693587 6 201601 0