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
123375173 12337517 3 F 20150224 20160622 20160505 20160705 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-030427 BRISTOL MYERS SQUIBB 84.00 YR F Y 0.00000 20160705 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
123375173 12337517 1 PS COUMADIN WARFARIN SODIUM 1 Unknown U 9218 TABLET
123375173 12337517 2 SS KETOROLAC TROMETHAMINE PHYSICIAN PARTNER KETOROLAC TROMETHAMINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123375173 12337517 1 Atrial fibrillation
123375173 12337517 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123375173 12337517 DE
123375173 12337517 OT
123375173 12337517 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123375173 12337517 Acute respiratory failure
123375173 12337517 Chronic obstructive pulmonary disease
123375173 12337517 International normalised ratio increased
123375173 12337517 Osteoporosis
123375173 12337517 Pain
123375173 12337517 Paraplegia
123375173 12337517 Spinal cord haemorrhage
123375173 12337517 Spinal fracture
123375173 12337517 Transient ischaemic attack
123375173 12337517 Vertebroplasty

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

no results found

Therapies reported

no results found