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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125439182 | 12543918 | 2 | F | 20160609 | 20160919 | 20160711 | 20160921 | EXP | DE-ROCHE-1789782 | ROCHE | 45.00 | YR | F | Y | 81.00000 | KG | 20160921 | MD | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125439182 | 12543918 | 1 | PS | Trastuzumab | TRASTUZUMAB | 1 | Subcutaneous | MOST RECENT DOSE : 09/JUN/2016 AND 28/JUN/2016 | 1150353 | 103792 | 600 | MG | SOLUTION FOR INJECTION | ||||||
| 125439182 | 12543918 | 2 | SS | EPIRUBICIN | EPIRUBICIN | 1 | Intravenous (not otherwise specified) | MOST RECENT DOSE : 17/NOV/2015 | 0 | 90 | MG/M**2 | ||||||||
| 125439182 | 12543918 | 3 | SS | CYCLOPHOSPHAMIDE. | CYCLOPHOSPHAMIDE | 1 | Intravenous (not otherwise specified) | MOST RECENT DOSE : 17/NOV/2015 | 0 | 900 | MG/M**2 | ||||||||
| 125439182 | 12543918 | 4 | SS | DOCETAXEL. | DOCETAXEL | 1 | Intravenous (not otherwise specified) | MOST RECENT DOSE : 25/JAN/2016 AND 26/JAN/2016 | 0 | 75 | MG/M**2 | ||||||||
| 125439182 | 12543918 | 5 | SS | TAMOXIFEN | TAMOXIFEN | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125439182 | 12543918 | 1 | HER-2 positive breast cancer |
| 125439182 | 12543918 | 2 | HER-2 positive breast cancer |
| 125439182 | 12543918 | 3 | HER-2 positive breast cancer |
| 125439182 | 12543918 | 4 | HER-2 positive breast cancer |
| 125439182 | 12543918 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125439182 | 12543918 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125439182 | 12543918 | Gait disturbance | |
| 125439182 | 12543918 | Headache |
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 |
|---|---|---|---|---|---|---|
| 125439182 | 12543918 | 1 | 20160223 | 0 | ||
| 125439182 | 12543918 | 2 | 20151006 | 0 | ||
| 125439182 | 12543918 | 3 | 20151006 | 0 | ||
| 125439182 | 12543918 | 4 | 20151208 | 0 | ||
| 125439182 | 12543918 | 5 | 20160210 | 0 |