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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119959243 | 11995924 | 3 | F | 20160530 | 20160802 | 20160203 | 20160804 | EXP | PHEH2016US002621 | NOVARTIS | 63.92 | YR | F | Y | 0.00000 | 20160804 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119959243 | 11995924 | 1 | PS | AFINITOR | EVEROLIMUS | 1 | Oral | 10 MG, QD | 22334 | 10 | MG | QD | |||||||
| 119959243 | 11995924 | 2 | SS | AROMASIN | EXEMESTANE | 1 | Oral | 25 MG, QD | 0 | 25 | MG | QD | |||||||
| 119959243 | 11995924 | 3 | C | LOVENOX | ENOXAPARIN SODIUM | 1 | Unknown | U | 0 | ||||||||||
| 119959243 | 11995924 | 4 | C | LISINOPRIL. | LISINOPRIL | 1 | Unknown | U | 0 | ||||||||||
| 119959243 | 11995924 | 5 | C | PROCHLORPERAZINE. | PROCHLORPERAZINE | 1 | Unknown | U | 0 | ||||||||||
| 119959243 | 11995924 | 6 | C | DOCUSATE | DOCUSATE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119959243 | 11995924 | 1 | Breast cancer |
| 119959243 | 11995924 | 2 | Breast cancer |
| 119959243 | 11995924 | 3 | Product used for unknown indication |
| 119959243 | 11995924 | 4 | Product used for unknown indication |
| 119959243 | 11995924 | 5 | Product used for unknown indication |
| 119959243 | 11995924 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 119959243 | 11995924 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119959243 | 11995924 | Epistaxis | |
| 119959243 | 11995924 | Full blood count decreased | |
| 119959243 | 11995924 | Gingival bleeding | |
| 119959243 | 11995924 | Malaise | |
| 119959243 | 11995924 | 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 |
|---|---|---|---|---|---|---|
| 119959243 | 11995924 | 1 | 20150923 | 0 | ||
| 119959243 | 11995924 | 2 | 20150923 | 0 |