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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125374152 | 12537415 | 2 | F | 20160708 | 20160707 | 20160715 | EXP | AU-INDIVIOR LIMITED-INDV-091828-2016 | INDIVIOR | 30.00 | YR | M | Y | 0.00000 | 20160715 | OT | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125374152 | 12537415 | 1 | PS | SUBOXONE | BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE | 1 | Unknown | 20MG/DAILY | Y | U | UNKNOWN | 22410 | |||||||
| 125374152 | 12537415 | 2 | SS | ALCOHOL. | ALCOHOL | 1 | Oral | UP TO 18 GRAMS | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125374152 | 12537415 | 1 | Product used for unknown indication |
| 125374152 | 12537415 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125374152 | 12537415 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125374152 | 12537415 | Alcohol abuse | |
| 125374152 | 12537415 | Chest pain | |
| 125374152 | 12537415 | Dyspnoea | |
| 125374152 | 12537415 | Hypersensitivity | |
| 125374152 | 12537415 | Vertigo | |
| 125374152 | 12537415 | Vision blurred |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |