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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123917723 | 12391772 | 3 | F | 20140415 | 20160913 | 20160522 | 20160916 | EXP | IT-ROCHE-1761078 | ROCHE | 78.59 | YR | F | Y | 60.00000 | KG | 20160916 | OT | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123917723 | 12391772 | 1 | PS | HERCEPTIN | TRASTUZUMAB | 1 | Intravenous (not otherwise specified) | 150 MG-VIAL FOR INTRAVENOUS USE | 103792 | 6 | MG/KG | SOLUTION FOR INFUSION | |||||||
| 123917723 | 12391772 | 2 | SS | HERCEPTIN | TRASTUZUMAB | 1 | Intravenous (not otherwise specified) | 150 MG-VIAL FOR INTRAVENOUS USE | 103792 | SOLUTION FOR INFUSION | |||||||||
| 123917723 | 12391772 | 3 | SS | HERCEPTIN | TRASTUZUMAB | 1 | Subcutaneous | 600 MG/5 ML-6 ML VIAL (GLASS) - 1 VIAL | U | 103792 | 600 | MG | SOLUTION FOR INJECTION | ||||||
| 123917723 | 12391772 | 4 | SS | NAVELBINE | VINORELBINE TARTRATE | 1 | Oral | 20 MG SOFT CAPSULES' 1 CAPSULE | 0 | 90 | MG | CAPSULE | |||||||
| 123917723 | 12391772 | 5 | C | COMBISARTAN | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123917723 | 12391772 | 1 | HER-2 positive breast cancer |
| 123917723 | 12391772 | 3 | HER-2 positive breast cancer |
| 123917723 | 12391772 | 4 | Breast cancer |
| 123917723 | 12391772 | 5 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123917723 | 12391772 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123917723 | 12391772 | Arthralgia | |
| 123917723 | 12391772 | Bone pain | |
| 123917723 | 12391772 | Cardiac failure | |
| 123917723 | 12391772 | Chest pain | |
| 123917723 | 12391772 | Cough | |
| 123917723 | 12391772 | Diarrhoea | |
| 123917723 | 12391772 | Dyspnoea | |
| 123917723 | 12391772 | Ejection fraction decreased | |
| 123917723 | 12391772 | Odynophagia | |
| 123917723 | 12391772 | Pain | |
| 123917723 | 12391772 | Pain in extremity | |
| 123917723 | 12391772 | 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 |
|---|---|---|---|---|---|---|
| 123917723 | 12391772 | 1 | 20140204 | 0 | ||
| 123917723 | 12391772 | 2 | 2015 | 20160609 | 0 | |
| 123917723 | 12391772 | 3 | 20150505 | 20150603 | 0 | |
| 123917723 | 12391772 | 4 | 20140619 | 20140929 | 0 |