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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114474833 | 11447483 | 3 | F | 19980806 | 20160627 | 20150902 | 20160830 | PER | US-JNJFOC-20150723476 | JANSSEN | 6.71 | YR | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114474833 | 11447483 | 1 | SS | RISPERDAL | RISPERIDONE | 1 | Oral | U | UNKNOWN | 0 | TABLETS | ||||||||
114474833 | 11447483 | 2 | PS | RISPERDAL | RISPERIDONE | 1 | Oral | U | UNKNOWN | 20272 | TABLETS | ||||||||
114474833 | 11447483 | 3 | SS | RISPERIDONE. | RISPERIDONE | 1 | Oral | U | 0 | TABLETS |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
114474833 | 11447483 | 1 | Bipolar disorder |
114474833 | 11447483 | 2 | Bipolar disorder |
114474833 | 11447483 | 3 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
114474833 | 11447483 | Drug ineffective | |
114474833 | 11447483 | Emotional disorder | |
114474833 | 11447483 | Enuresis | |
114474833 | 11447483 | Gynaecomastia | |
114474833 | 11447483 | Obesity |
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 |
---|---|---|---|---|---|---|
114474833 | 11447483 | 2 | 200101 | 200105 | 0 |