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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125282961 | 12528296 | 1 | I | 20160628 | 20160705 | 20160705 | EXP | US-INDIVIOR LIMITED-INDV-091813-2016 | INDIVIOR | 47.00 | YR | M | Y | 0.00000 | 20160705 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125282961 | 12528296 | 1 | PS | SUBOXONE | BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE | 1 | Sublingual | UNK | UNKNOWN | 22410 | |||||||||
125282961 | 12528296 | 2 | SS | SUBOXONE | BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE | 1 | Sublingual | 1.5 - 2 MG DAILY | UNKNOWN | 22410 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125282961 | 12528296 | 1 | Drug dependence |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125282961 | 12528296 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125282961 | 12528296 | Fall | |
125282961 | 12528296 | Limb crushing injury | |
125282961 | 12528296 | Product preparation error |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |