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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125228461 | 12522846 | 1 | I | 20160329 | 20160701 | 20160701 | EXP | PHHY2016RU041817 | NOVARTIS | 67.00 | YR | F | Y | 0.00000 | 20160701 | CN | COUNTRY NOT SPECIFIED | RU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125228461 | 12522846 | 1 | PS | AFINITOR | EVEROLIMUS | 1 | Unknown | 10 MG, QD | 22334 | 10 | MG | QD | |||||||
| 125228461 | 12522846 | 2 | SS | AFINITOR | EVEROLIMUS | 1 | 22334 | ||||||||||||
| 125228461 | 12522846 | 3 | SS | AFINITOR | EVEROLIMUS | 1 | 22334 | ||||||||||||
| 125228461 | 12522846 | 4 | C | AROMASIN | EXEMESTANE | 1 | Unknown | 0 | |||||||||||
| 125228461 | 12522846 | 5 | C | HEPA-MERZ | 2 | Unknown | 0 | ||||||||||||
| 125228461 | 12522846 | 6 | C | MOTILIUM | DOMPERIDONE | 1 | Unknown | 0 | |||||||||||
| 125228461 | 12522846 | 7 | C | SMECTA | MONTMORILLONITE | 1 | Unknown | 0 | |||||||||||
| 125228461 | 12522846 | 8 | C | GAVICON /01291401/ | 2 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125228461 | 12522846 | 1 | Breast cancer |
| 125228461 | 12522846 | 2 | Fallopian tube cancer |
| 125228461 | 12522846 | 3 | Metastases to liver |
| 125228461 | 12522846 | 4 | Product used for unknown indication |
| 125228461 | 12522846 | 5 | Product used for unknown indication |
| 125228461 | 12522846 | 6 | Product used for unknown indication |
| 125228461 | 12522846 | 7 | Product used for unknown indication |
| 125228461 | 12522846 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125228461 | 12522846 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125228461 | 12522846 | Anxiety | |
| 125228461 | 12522846 | Asthenia | |
| 125228461 | 12522846 | Death | |
| 125228461 | 12522846 | Diarrhoea | |
| 125228461 | 12522846 | Dysgeusia | |
| 125228461 | 12522846 | Eating disorder | |
| 125228461 | 12522846 | Mood altered | |
| 125228461 | 12522846 | Product use issue | |
| 125228461 | 12522846 | Somnolence | |
| 125228461 | 12522846 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |