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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127905691 | 12790569 | 1 | I | 20160927 | 20160929 | 20160929 | EXP | GB-ROCHE-1836291 | ROCHE | 51.00 | YR | Y | 0.00000 | 20160929 | MD | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127905691 | 12790569 | 1 | PS | Trastuzumab | TRASTUZUMAB | 1 | Unknown | U | 103792 | ||||||||||
| 127905691 | 12790569 | 2 | SS | Pertuzumab | PERTUZUMAB | 1 | Unknown | U | 125409 | SOLUTION FOR INFUSION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127905691 | 12790569 | 1 | Product used for unknown indication |
| 127905691 | 12790569 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127905691 | 12790569 | OT |
| 127905691 | 12790569 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127905691 | 12790569 | Arthralgia | |
| 127905691 | 12790569 | Dehydration | |
| 127905691 | 12790569 | Diarrhoea | |
| 127905691 | 12790569 | Fatigue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |