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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121983962 | 12198396 | 2 | F | 2004 | 20160627 | 20160322 | 20160830 | PER | US-JNJFOC-20160311933 | JANSSEN | 0.00 | C | M | Y | 0.00000 | 20160830 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121983962 | 12198396 | 1 | PS | RISPERDAL | RISPERIDONE | 1 | Oral | IN VARYING DOSES OF 0.25, 0.5 AND 1 MG | U | U | 20272 | TABLETS | |||||||
| 121983962 | 12198396 | 2 | SS | RISPERIDONE. | RISPERIDONE | 1 | Unknown | U | 0 | TABLETS |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121983962 | 12198396 | 1 | Attention deficit/hyperactivity disorder |
| 121983962 | 12198396 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121983962 | 12198396 | Abnormal weight gain | |
| 121983962 | 12198396 | Gynaecomastia | |
| 121983962 | 12198396 | Off label use | |
| 121983962 | 12198396 | Product use issue |
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 |
|---|---|---|---|---|---|---|
| 121983962 | 12198396 | 1 | 2004 | 2009 | 0 |