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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127001192 | 12700119 | 2 | F | 20150811 | 20160823 | 20160830 | 20160906 | EXP | PL-PFIZER INC-2015268911 | PFIZER | 43.00 | YR | F | Y | 61.00000 | KG | 20160906 | MD | PL | PL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127001192 | 12700119 | 1 | PS | CARBOPLATIN. | CARBOPLATIN | 1 | Intravenous (not otherwise specified) | 690 MG (AUC 6), EVERY 21 DAYS | 76517 | 690 | MG | Q3W | |||||||
| 127001192 | 12700119 | 2 | SS | DOCETAXEL. | DOCETAXEL | 1 | Intravenous (not otherwise specified) | 122 MG, EVERY 21 DAYS | 202356 | 122 | MG | Q3W | |||||||
| 127001192 | 12700119 | 3 | SS | TRASTUZUMAB | TRASTUZUMAB | 1 | Intravenous (not otherwise specified) | 456 MG, EVERY 21 DAYS | 0 | 456 | MG | POWDER FOR SOLUTION FOR INFUSION | |||||||
| 127001192 | 12700119 | 4 | C | DEXAVEN | DEXAMETHASONE | 1 | Intravenous (not otherwise specified) | DOSE:2 X 8 MG, REGIMEN:EVERY 21 DAYS | 0 | 8 | MG | ||||||||
| 127001192 | 12700119 | 5 | C | ONDASETRON | ONDANSETRON | 1 | Intravenous (not otherwise specified) | DOSE:2 X 8 MG,REGIMEN: EVERY 21 DAYS | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127001192 | 12700119 | 1 | Breast cancer |
| 127001192 | 12700119 | 2 | Breast cancer |
| 127001192 | 12700119 | 3 | Breast cancer |
| 127001192 | 12700119 | 4 | Antiallergic therapy |
| 127001192 | 12700119 | 5 | Prophylaxis of nausea and vomiting |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127001192 | 12700119 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127001192 | 12700119 | Dehydration | |
| 127001192 | 12700119 | Neutropenia |
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 |
|---|---|---|---|---|---|---|
| 127001192 | 12700119 | 1 | 20150804 | 0 | ||
| 127001192 | 12700119 | 2 | 20150804 | 0 | ||
| 127001192 | 12700119 | 3 | 20150804 | 0 | ||
| 127001192 | 12700119 | 4 | 20150804 | 20150804 | 0 | |
| 127001192 | 12700119 | 5 | 20150804 | 20150804 | 0 |