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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7914580 | 8244855 | F | 7914580-2 | 20110927 | 20111101 | 20111115 | EXP | PHEH2011US05369 | NOVARTIS PHARMACEUTICAL CORPORATION | 24 | YR | M | Y | 20111115 | CN | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7914580 | 1018048298 | C | TOPAMAX | 1 | |||||||
| 7914580 | 1018048299 | C | LAMICTAL | 1 | |||||||
| 7914580 | 1018048300 | C | CLONIDINE | 1 | |||||||
| 7914580 | 1018048294 | PS | AFINITOR | 1 | 5 MG, UNK | 022334 | |||||
| 7914580 | 1018048295 | SS | AFINITOR | 1 | ORAL | 5 MG, MONDAY TO SATURDAY | 022334 | ||||
| 7914580 | 1018048296 | SS | AFINITOR | 1 | 5 MG, DAILY | 022334 | |||||
| 7914580 | 1018048297 | C | DEPAKOTE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7914580 | 1018048294 | ASTROCYTOMA, LOW GRADE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7914580 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7914580 | DRUG LEVEL BELOW THERAPEUTIC |
| 7914580 | CONVULSION |
| 7914580 | CONTUSION |
| 7914580 | SCRATCH |
| 7914580 | DIARRHOEA |
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 |
|---|---|---|---|---|---|
| 7914580 | 1018048294 | 20110611 | |||
| 7914580 | 1018048295 | 20110917 | |||
| 7914580 | 1018048296 | 20111025 |