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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6918680 | 7491477 | F | 6918680-5 | 20100729 | 20100811 | EXP | PHFR2010GB01282 | NOVARTIS PHARMACEUTICAL CORPORATION | YR | M | Y | 20100811 | MD | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6918680 | 1014390752 | PS | CLOZARIL | 1 | ORAL | UNK | 019758 | ||||
| 6918680 | 1014390753 | SS | LORAZEPAM | 1 | 7 X 1MG |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6918680 | 1014390752 | SCHIZOPHRENIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6918680 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6918680 | CONFUSIONAL STATE |
| 6918680 | INCOHERENT |
| 6918680 | OVERDOSE |
| 6918680 | TACHYCARDIA |
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 |
|---|---|---|---|---|---|
| 6918680 | 1014390752 | 20090216 |