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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126423051 | 12642305 | 1 | I | 20160803 | 20160810 | 20160810 | EXP | BR-JNJFOC-20160805308 | JANSSEN | 0.00 | A | M | Y | 0.00000 | 20160810 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126423051 | 12642305 | 1 | PS | HALDOL | HALOPERIDOL | 1 | Unknown | N | 15923 | .5 | DF | TABLETS | QD | ||||||
| 126423051 | 12642305 | 2 | C | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Unknown | 0 | UNSPECIFIED | ||||||||||
| 126423051 | 12642305 | 3 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | Unknown | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126423051 | 12642305 | 1 | Stress |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126423051 | 12642305 | OT |
| 126423051 | 12642305 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126423051 | 12642305 | Asthenia | |
| 126423051 | 12642305 | Depression | |
| 126423051 | 12642305 | Intentional self-injury | |
| 126423051 | 12642305 | Off label use | |
| 126423051 | 12642305 | Pain in extremity | |
| 126423051 | 12642305 | Product use issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |