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
120574412 12057441 2 F 20151223 20160812 20160210 20160824 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-005366 BRISTOL MYERS SQUIBB 54.74 YR F Y 0.00000 20160824 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
120574412 12057441 1 PS COUMADIN WARFARIN SODIUM 1 Oral 5 MG, QD Y 9218 5 MG TABLET QD
120574412 12057441 2 C PARACETAMOL ACETAMINOPHEN 1 Unknown 1 G, UNK U 0 1 G
120574412 12057441 3 C ANTRA /00661201/ OMEPRAZOLE 1 Oral 1 UNIT, UNK U 0 1 DF SOLUTION FOR INFUSION
120574412 12057441 4 C TORA-DOL KETOROLAC TROMETHAMINE 1 Oral 10 MG, UNK U 0 10 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120574412 12057441 1 Venous thrombosis
120574412 12057441 2 Product used for unknown indication
120574412 12057441 3 Product used for unknown indication
120574412 12057441 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120574412 12057441 OT
120574412 12057441 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
120574412 12057441 Back injury
120574412 12057441 Decreased appetite
120574412 12057441 Fall
120574412 12057441 Haematoma evacuation
120574412 12057441 Head injury
120574412 12057441 Headache
120574412 12057441 Subdural haematoma

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found