Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117144563 | 11714456 | 3 | F | 20151019 | 20160831 | 20151109 | 20160908 | EXP | PHEH2015US022097 | NOVARTIS | 12.10 | YR | M | Y | 0.00000 | 20160908 | CN | COUNTRY NOT SPECIFIED | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117144563 | 11714456 | 1 | PS | AFINITOR | EVEROLIMUS | 1 | Oral | 12.5 MG, QD | 3750.31592 | MG | Y | 22334 | 12.5 | MG | TABLET | QD | |||
| 117144563 | 11714456 | 2 | SS | AFINITOR | EVEROLIMUS | 1 | 3750.31592 | MG | Y | 22334 | TABLET | ||||||||
| 117144563 | 11714456 | 3 | C | TOPAMAX | TOPIRAMATE | 1 | Unknown | U | 0 | ||||||||||
| 117144563 | 11714456 | 4 | C | LAMICTAL | LAMOTRIGINE | 1 | Unknown | U | 0 | ||||||||||
| 117144563 | 11714456 | 5 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Unknown | U | 0 | ||||||||||
| 117144563 | 11714456 | 6 | C | IBUPROFEN. | IBUPROFEN | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117144563 | 11714456 | 1 | Ganglioglioma |
| 117144563 | 11714456 | 2 | Astrocytoma, low grade |
| 117144563 | 11714456 | 3 | Product used for unknown indication |
| 117144563 | 11714456 | 4 | Product used for unknown indication |
| 117144563 | 11714456 | 5 | Product used for unknown indication |
| 117144563 | 11714456 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117144563 | 11714456 | HO |
| 117144563 | 11714456 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117144563 | 11714456 | Decreased appetite | |
| 117144563 | 11714456 | Fall | |
| 117144563 | 11714456 | Head injury | |
| 117144563 | 11714456 | Mouth ulceration | |
| 117144563 | 11714456 | Seizure | |
| 117144563 | 11714456 | Stomatitis | |
| 117144563 | 11714456 | Underweight |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 117144563 | 11714456 | 1 | 20150512 | 20160828 | 0 |