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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125993001 | 12599300 | 1 | I | 20160725 | 20160727 | 20160727 | EXP | CA-JNJFOC-20160720782 | JANSSEN | 32.00 | YR | A | M | Y | 110.22000 | KG | 20160727 | CN | CA | CA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125993001 | 12599300 | 1 | PS | INVEGA SUSTENNA | PALIPERIDONE PALMITATE | 1 | Intramuscular | U | U | 22264 | INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125993001 | 12599300 | 1 | Bipolar disorder |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125993001 | 12599300 | DS |
125993001 | 12599300 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125993001 | 12599300 | Alopecia | |
125993001 | 12599300 | Decreased interest | |
125993001 | 12599300 | Obesity | |
125993001 | 12599300 | Off label use | |
125993001 | 12599300 | Product use issue | |
125993001 | 12599300 | Suicidal ideation | |
125993001 | 12599300 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |