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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6138789 | 6957016 | I | 6138789-6 | 20090106 | 20090323 | 20090331 | EXP | PHHY2009CA11040 | NOVARTIS PHARMACEUTICALS CORP. | 66 | F | Y | 20090331 | PH | CANADA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6138789 | 1011359253 | PS | CLOZARIL | 1 | UNK | 019758 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6138789 | 1011359253 | SCHIZOPHRENIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6138789 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6138789 | ANTIPSYCHOTIC DRUG LEVEL INCREASED |
| 6138789 | CERVICAL VERTEBRAL FRACTURE |
| 6138789 | FALL |
| 6138789 | HIP FRACTURE |
| 6138789 | INFECTION |
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 |
|---|---|---|---|---|---|
| 6138789 | 1011359253 | 20050816 |