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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124942792 | 12494279 | 2 | F | 20160325 | 20160627 | 20160623 | 20160705 | EXP | PHHO2016NO005740 | NOVARTIS | 59.00 | YR | F | Y | 69.98000 | KG | 20160705 | MD | NO | NO |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124942792 | 12494279 | 1 | PS | AFINITOR | EVEROLIMUS | 1 | Oral | 10 OT | Y | 22334 | |||||||||
| 124942792 | 12494279 | 2 | SS | EXEMESTANE. | EXEMESTANE | 1 | Unknown | UNK | Y | 0 | |||||||||
| 124942792 | 12494279 | 3 | SS | AROMASIN | EXEMESTANE | 1 | Oral | 25 MG, QD | U | 0 | 25 | MG | QD | ||||||
| 124942792 | 12494279 | 4 | C | CALCIGRAN FORTE | 2 | Unknown | 1000 MG/800 IE (SEVERAL YEARS) | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124942792 | 12494279 | 1 | Breast cancer metastatic |
| 124942792 | 12494279 | 2 | Breast cancer metastatic |
| 124942792 | 12494279 | 3 | Product used for unknown indication |
| 124942792 | 12494279 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124942792 | 12494279 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124942792 | 12494279 | Abdominal pain | |
| 124942792 | 12494279 | Alanine aminotransferase increased | |
| 124942792 | 12494279 | Aspartate aminotransferase increased | |
| 124942792 | 12494279 | Diarrhoea | |
| 124942792 | 12494279 | Gastritis | |
| 124942792 | 12494279 | Haemoglobin increased | |
| 124942792 | 12494279 | Hypokalaemia | |
| 124942792 | 12494279 | Lymphocyte count decreased | |
| 124942792 | 12494279 | Nausea | |
| 124942792 | 12494279 | Stomatitis | |
| 124942792 | 12494279 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 124942792 | 12494279 | 1 | 20160322 | 20160412 | 0 | |
| 124942792 | 12494279 | 2 | 20160322 | 20160412 | 0 |