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
127297391 12729739 1 I 20160817 20160901 20160909 20160909 EXP FR-INDIVIOR LIMITED-INDV-094577-2016 INDIVIOR 43.00 YR M Y 0.00000 20160909 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
127297391 12729739 1 PS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Unknown UNK Y UNKNOWN 20732 SUBLINGUAL TABLET
127297391 12729739 2 SS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 4 MG, QID Y UNKNOWN 20732 4 MG SUBLINGUAL TABLET QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127297391 12729739 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127297391 12729739 HO
127297391 12729739 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127297391 12729739 Aortic disorder
127297391 12729739 Cardiac failure
127297391 12729739 Drug dependence
127297391 12729739 Erysipelas
127297391 12729739 Intentional product misuse

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
127297391 12729739 2 1998 0