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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7788516 | 8163091 | I | 7788516-1 | 20110831 | 20110927 | 20110930 | EXP | PHHO2011US15502 | NOVARTIS PHARMACEUTICAL CORPORATION | YR | F | Y | 57 | KG | 20110929 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7788516 | 1017675146 | PS | AFINITOR | 1 | ORAL | UNK | 022334 | ||||
| 7788516 | 1017675147 | SS | TEMOZOLOMIDE | 1 | UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7788516 | 1017675146 | GLIOBLASTOMA |
| 7788516 | 1017675147 | GLIOBLASTOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7788516 | DE |
| 7788516 | OT |
| 7788516 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7788516 | LUNG INFECTION |
| 7788516 | PLATELET COUNT DECREASED |
| 7788516 | WHITE BLOOD CELL COUNT DECREASED |
| 7788516 | FEBRILE NEUTROPENIA |
| 7788516 | LYMPHOCYTE COUNT DECREASED |
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 |
|---|---|---|---|---|---|
| 7788516 | 1017675146 | 20110803 | 20110831 | 29 | DAY |
| 7788516 | 1017675147 | 20110803 | 20110831 | 29 | DAY |