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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5374943 | 6345948 | I | 5374943-9 | 20070621 | 20070629 | EXP | PHNR2007AU01286 | NOVARTIS PHARMACEUTICALS CORP. | M | Y | 20070629 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5374943 | 1008647754 | PS | CLOZARIL | 1 | ORAL | 75-450MG DAILY | 019758 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5374943 | 1008647754 | SCHIZOPHRENIA |
Outcome of event
Event ID | OUTC COD |
---|---|
5374943 | OT |
Reactions reported
Event ID | PT |
---|---|
5374943 | CHOKING |
5374943 | SALIVARY HYPERSECRETION |
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 |
---|---|---|---|---|---|
5374943 | 1008647754 | 20061207 |