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
125617702 12561770 2 F 20160607 20160824 20160715 20160831 EXP JP-SA-2016SA128006 AVENTIS 88.00 YR E M Y 47.50000 KG 20160831 MD JP JP

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
125617702 12561770 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Oral Y U 20839 75 MG TABLET QD
125617702 12561770 2 C FUROSEMIDE. FUROSEMIDE 1 Oral 0 40 MG QD
125617702 12561770 3 C BAYASPIRIN ASPIRIN 1 Oral 0 100 MG QD
125617702 12561770 4 C TANATRIL IMIDAPRIL 1 0
125617702 12561770 5 C ARTIST CARVEDILOL 1 0
125617702 12561770 6 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 0 20 MG QD
125617702 12561770 7 C CARDENALIN DOXAZOSIN MESYLATE 1 Oral 0 2 MG QD
125617702 12561770 8 C CONIEL BENIDIPINE HYDROCHLORIDE 1 Oral 0 4 MG BID

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125617702 12561770 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125617702 12561770 Thrombocytopenia

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
125617702 12561770 1 20160419 20160717 0
125617702 12561770 7 20160525 0
125617702 12561770 8 20160608 0