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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7584791 | 8017702 | I | 7584791-7 | 20110621 | 20110630 | EXP | PHHY2011TW55456 | NOVARTIS PHARMACEUTICAL CORPORATION | 26 | YR | F | Y | 20110630 | OT | TAIWAN, PROVINCE OF CHINA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7584791 | 1016909634 | SS | CLOZAPINE | 1 | 50 MG, DAILY | 019758 | |||||
| 7584791 | 1016909638 | C | BIPERIDEN HYDROCHLORIDE TAB | 1 | 2 MG, DAILY | ||||||
| 7584791 | 1016909633 | PS | CLOZAPINE | 1 | 12.5 MG, DAILY | 019758 | |||||
| 7584791 | 1016909637 | C | BIPERIDEN HYDROCHLORIDE TAB | 1 | 4 MG, DAILY | ||||||
| 7584791 | 1016909635 | SS | CLOZAPINE | 1 | 25 MG, DAILY | 019758 | |||||
| 7584791 | 1016909636 | C | BIPERIDEN HYDROCHLORIDE TAB | 1 | 2 MG, DAILY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7584791 | 1016909633 | SCHIZOPHRENIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7584791 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7584791 | MYASTHENIA GRAVIS |
| 7584791 | HEART RATE INCREASED |
| 7584791 | DYSPHAGIA |
| 7584791 | DYSKINESIA |
| 7584791 | RESPIRATORY FAILURE |
| 7584791 | RESPIRATORY ACIDOSIS |
| 7584791 | DROOLING |
| 7584791 | EYELID PTOSIS |
| 7584791 | PSYCHOTIC DISORDER |
| 7584791 | DYSPHONIA |
| 7584791 | SINUS TACHYCARDIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |