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
126817311 12681731 1 I 2012 20160816 20160824 20160824 EXP FR-INDIVIOR LIMITED-INDV-093912-2016 INDIVIOR 40.00 YR M Y 0.00000 20160824 OT FR FR

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
126817311 12681731 1 PS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 4MG PER DAY FOR 4 YEARS Y UNKNOWN 20732 SUBLINGUAL TABLET
126817311 12681731 2 SS SKENAN MORPHINE SULFATE 1 Intravenous (not otherwise specified) 600 MG, DAILY Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126817311 12681731 1 Product used for unknown indication
126817311 12681731 2 Pain

Outcome of event

Event ID CASEID OUTC COD
126817311 12681731 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126817311 12681731 Arthritis bacterial
126817311 12681731 Intentional product use issue
126817311 12681731 Osteonecrosis

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
126817311 12681731 1 2012 2016 0
126817311 12681731 2 2016 2016 0