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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120919745 | 12091974 | 5 | F | 20160212 | 20160823 | 20160219 | 20160829 | PER | PHEH2016US004006 | NOVARTIS | 83.18 | YR | F | Y | 0.00000 | 20160829 | OT | US | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120919745 | 12091974 | 1 | PS | AFINITOR | EVEROLIMUS | 1 | Oral | 5 MG, QD | N | F0049 | 22334 | 5 | MG | TABLET | QD | ||||
| 120919745 | 12091974 | 2 | SS | AFINITOR | EVEROLIMUS | 1 | Oral | 7.5 MG, QD | N | F0049 | 22334 | 7.5 | MG | TABLET | QD | ||||
| 120919745 | 12091974 | 3 | SS | AFINITOR | EVEROLIMUS | 1 | Oral | 7.5 MG, QD | N | F0026 | 22334 | 7.5 | MG | TABLET | QD | ||||
| 120919745 | 12091974 | 4 | SS | AFINITOR | EVEROLIMUS | 1 | Oral | 5 MG, QD | N | F0029 | 22334 | 5 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120919745 | 12091974 | 1 | Breast cancer |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120919745 | 12091974 | Cough | |
| 120919745 | 12091974 | Genital pain | |
| 120919745 | 12091974 | Gingival pain | |
| 120919745 | 12091974 | Joint swelling | |
| 120919745 | 12091974 | Malignant neoplasm progression | |
| 120919745 | 12091974 | Oral pain |
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 |
|---|---|---|---|---|---|---|
| 120919745 | 12091974 | 1 | 20160210 | 0 |