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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125812171 | 12581217 | 1 | I | 20160715 | 20160721 | 20160721 | EXP | US-ETHYPHARM USA CORP-EY-BP-US-2016-033 | ETHYPHARM | 20.00 | YR | UNK | Y | 62.20000 | KG | 20160720 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125812171 | 12581217 | 1 | PS | SUBUTEX | BUPRENORPHINE HYDROCHLORIDE | 1 | 0.5 TO 1.5 MG | 90622 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125812171 | 12581217 | 1 | Substance use |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125812171 | 12581217 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125812171 | 12581217 | Depression | |
| 125812171 | 12581217 | Drug abuse | |
| 125812171 | 12581217 | Euphoric mood | |
| 125812171 | 12581217 | Intentional product misuse | |
| 125812171 | 12581217 | Intentional product use issue | |
| 125812171 | 12581217 | Somnolence | |
| 125812171 | 12581217 | Suicidal ideation |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |