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
126577071 12657707 1 I 20160715 20160804 20160816 20160816 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-064292 BRISTOL MYERS SQUIBB 86.71 YR F Y 60.00000 KG 20160816 CN IT IT

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
126577071 12657707 1 PS COUMADIN WARFARIN SODIUM 1 Oral 5 MG, UNK Y 9218 5 MG TABLET
126577071 12657707 2 C VALSARTAN. VALSARTAN 1 Oral 40 MG, UNK U 0 40 MG
126577071 12657707 3 C NORVASC AMLODIPINE BESYLATE 1 Oral 10 MG, UNK U 0 10 MG
126577071 12657707 4 C LASIX FUROSEMIDE 1 Oral 100 MG, UNK U 0 100 MG
126577071 12657707 5 C PANTORC PANTOPRAZOLE SODIUM 1 Oral 40 MG, UNK U 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126577071 12657707 1 Atrial fibrillation
126577071 12657707 2 Hypertension
126577071 12657707 3 Hypertension
126577071 12657707 4 Polyuria
126577071 12657707 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126577071 12657707 HO
126577071 12657707 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126577071 12657707 Accidental overdose
126577071 12657707 Anaemia
126577071 12657707 Packed red blood cell transfusion

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
126577071 12657707 1 20070101 0
126577071 12657707 2 20160801 0
126577071 12657707 3 20160801 0
126577071 12657707 4 20160801 0
126577071 12657707 5 20160801 0