Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6733700 | 7394375 | F | 6733700-9 | 20100401 | 20100506 | 20100520 | EXP | PHHY2010AU21019 | NOVARTIS PHARMACEUTICAL CORPORATION | 27 | YR | M | Y | 90 | KG | 20100520 | OT | AUSTRALIA |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6733700 | 1013720727 | PS | CLOZARIL | 1 | ORAL | 200 MG, UNK | 019758 | ||||
| 6733700 | 1013720728 | C | AMISULPRIDE | 2 | 200 MG DAILY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6733700 | 1013720727 | SCHIZOPHRENIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6733700 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6733700 | BLOOD PRESSURE INCREASED |
| 6733700 | CARDIAC FAILURE |
| 6733700 | CONDITION AGGRAVATED |
| 6733700 | CONFUSIONAL STATE |
| 6733700 | EJECTION FRACTION DECREASED |
| 6733700 | HALLUCINATION, AUDITORY |
| 6733700 | PARANOIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6733700 | 1013720727 | 20100211 | 20100406 | 55 | DAY |