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
125498821 12549882 1 I 201309 20160701 20160712 20160712 EXP FR-INDIVIOR LIMITED-INDV-091928-2016 INDIVIOR 41.40 YR M Y 0.00000 20160712 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
125498821 12549882 1 PS SUBUTEX BUPRENORPHINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) UNK Y U UNKNOWN 20732 SUBLINGUAL TABLET
125498821 12549882 2 SS SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 Unknown 2MG/0.5MG, 2 TABLETS IN THE MORNING AND ONE IN THE MIDDAY UNKNOWN 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125498821 12549882 1 Drug dependence
125498821 12549882 2 Drug dependence

Outcome of event

Event ID CASEID OUTC COD
125498821 12549882 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125498821 12549882 Deep vein thrombosis
125498821 12549882 Intentional product misuse
125498821 12549882 Intentional product use issue
125498821 12549882 Post thrombotic syndrome

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
125498821 12549882 1 201309 0
125498821 12549882 2 201506 0