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
122885993 12288599 3 F 20160831 20160421 20160912 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-028747 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160912 CN US 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
122885993 12288599 1 PS ELIQUIS APIXABAN 1 Unknown U 202155
122885993 12288599 2 SS LYRICA PREGABALIN 1 Unknown U 0
122885993 12288599 3 SS HYDROCODONE HYDROCODONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122885993 12288599 1 Cardiac disorder
122885993 12288599 2 Back pain
122885993 12288599 3 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122885993 12288599 Pain in extremity
122885993 12288599 Product use issue

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

no results found

Therapies reported

no results found