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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126695881 | 12669588 | 1 | I | 20140701 | 20160816 | 20160819 | 20160819 | EXP | GB-JNJFOC-20160814073 | JANSSEN | 38.00 | YR | A | F | Y | 63.00000 | KG | 20160819 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126695881 | 12669588 | 1 | PS | HALOPERIDOL. | HALOPERIDOL | 1 | Parenteral | DRUG ADMINISTERED FOR 32 DAYS??START PERIOD 2 DAYS | N | N | 15923 | UNSPECIFIED | |||||||
| 126695881 | 12669588 | 2 | SS | RISPERIDONE. | RISPERIDONE | 1 | Oral | DOSE INCREASED | N | 0 | UNSPECIFIED | ||||||||
| 126695881 | 12669588 | 3 | SS | RISPERIDONE. | RISPERIDONE | 1 | Oral | START PERIOD 2 DAYS, DOSE INCREASED | N | 20272 | 5 | DF | UNSPECIFIED | ||||||
| 126695881 | 12669588 | 4 | SS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Unknown | START PERIOD 1 DAY, DOSE REDUCED | N | 0 | 10 | DF | UNSPECIFIED | ||||||
| 126695881 | 12669588 | 5 | SS | ARIPIPRAZOLE. | ARIPIPRAZOLE | 1 | Unknown | DOSE REDUCED | N | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126695881 | 12669588 | 1 | Product used for unknown indication |
| 126695881 | 12669588 | 2 | Product used for unknown indication |
| 126695881 | 12669588 | 3 | Product used for unknown indication |
| 126695881 | 12669588 | 4 | Depression |
| 126695881 | 12669588 | 5 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126695881 | 12669588 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126695881 | 12669588 | Breast enlargement | |
| 126695881 | 12669588 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 126695881 | 12669588 | 1 | 20140629 | 20140731 | 0 | |
| 126695881 | 12669588 | 3 | 20140629 | 0 | ||
| 126695881 | 12669588 | 4 | 20140701 | 0 |