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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106335784 | 10633578 | 4 | F | 20160920 | 20141205 | 20160927 | EXP | US-JNJFOC-20141116209 | JANSSEN | 0.00 | A | M | Y | 0.00000 | 20160927 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106335784 | 10633578 | 1 | SS | RISPERDAL | RISPERIDONE | 1 | Oral | 2 MG ONE PILL AT BED TIME | U | U | 0 | TABLETS | |||||||
| 106335784 | 10633578 | 2 | PS | RISPERDAL | RISPERIDONE | 1 | Oral | 2 MG ONE PILL AT BED TIME | U | U | 20272 | TABLETS | |||||||
| 106335784 | 10633578 | 3 | SS | RISPERIDONE. | RISPERIDONE | 1 | Oral | U | 0 | TABLETS |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 106335784 | 10633578 | 1 | Psychotic disorder |
| 106335784 | 10633578 | 2 | Schizophrenia |
| 106335784 | 10633578 | 3 | Schizophrenia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 106335784 | 10633578 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 106335784 | 10633578 | Abnormal weight gain | |
| 106335784 | 10633578 | Galactorrhoea | |
| 106335784 | 10633578 | Gynaecomastia | |
| 106335784 | 10633578 | Hyperprolactinaemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |