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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126691983 | 12669198 | 3 | F | 201605 | 20160926 | 20160819 | 20160930 | EXP | US-JNJFOC-20160808634 | JANSSEN | 21.03 | YR | A | M | Y | 0.00000 | 20160930 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126691983 | 12669198 | 1 | PS | INVEGA SUSTENNA | PALIPERIDONE PALMITATE | 1 | Intramuscular | DAY ONE DOSE | Y | N | UNKNOWN | 22264 | 234 | MG | INJECTION | ||||
| 126691983 | 12669198 | 2 | SS | INVEGA | PALIPERIDONE | 1 | Oral | Y | N | UNKNOWN | 0 | OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET | |||||||
| 126691983 | 12669198 | 3 | SS | INVEGA | PALIPERIDONE | 1 | Oral | Y | N | UNKNOWN | 21999 | 12 | MG | OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET | QD | ||||
| 126691983 | 12669198 | 4 | C | LITHIUM. | LITHIUM | 1 | Oral | D | 0 | 600 | MG | UNSPECIFIED | BID | ||||||
| 126691983 | 12669198 | 5 | C | ATIVAN | LORAZEPAM | 1 | Oral | AT BEDTIME | D | 0 | UNSPECIFIED | ||||||||
| 126691983 | 12669198 | 6 | C | VALIUM | DIAZEPAM | 1 | Oral | AT BEDTIME | D | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126691983 | 12669198 | 1 | Product used for unknown indication |
| 126691983 | 12669198 | 2 | Product used for unknown indication |
| 126691983 | 12669198 | 3 | Product used for unknown indication |
| 126691983 | 12669198 | 4 | Affective disorder |
| 126691983 | 12669198 | 5 | Product used for unknown indication |
| 126691983 | 12669198 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126691983 | 12669198 | HO |
| 126691983 | 12669198 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126691983 | 12669198 | Anosognosia | |
| 126691983 | 12669198 | Catatonia | |
| 126691983 | 12669198 | Hospitalisation | |
| 126691983 | 12669198 | Parkinsonism | |
| 126691983 | 12669198 | Psychotic disorder | |
| 126691983 | 12669198 | Treatment noncompliance |
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 |
|---|---|---|---|---|---|---|
| 126691983 | 12669198 | 1 | 20160713 | 20160713 | 0 |