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
39238882 3923888 2 F 20030221 20160804 20030403 20160816 EXP US-BRISTOL-MYERS SQUIBB COMPANY-12226445 BRISTOL MYERS SQUIBB 81.47 YR F Y 70.00000 KG 20160816 CN IN US

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
39238882 3923888 1 PS COUMADIN WARFARIN SODIUM 1 Oral 5 MG, QD U 9218 5 MG TABLET QD
39238882 3923888 2 SS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Unknown U 0 SOLUTION FOR INFUSION
39238882 3923888 3 C VITAMIN D2 ERGOCALCIFEROL 1 Unknown U 0
39238882 3923888 4 C CALCIUM CARBONATE. CALCIUM CARBONATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
39238882 3923888 1 Product used for unknown indication
39238882 3923888 2 Product used for unknown indication
39238882 3923888 3 Product used for unknown indication
39238882 3923888 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
39238882 3923888 LT
39238882 3923888 OT
39238882 3923888 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
39238882 3923888 Coagulopathy
39238882 3923888 Diverticulum
39238882 3923888 Haematoma
39238882 3923888 Haemoglobin decreased
39238882 3923888 Haemorrhoids
39238882 3923888 Polypectomy
39238882 3923888 Rectal haemorrhage

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
39238882 3923888 1 1998 0