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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127980741 | 12798074 | 1 | I | 20100928 | 20110607 | 20160930 | 20160930 | EXP | US-ROCHE-783517 | ROCHE | 76.00 | YR | F | Y | 53.90000 | KG | 20160930 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127980741 | 12798074 | 1 | PS | Bevacizumab | BEVACIZUMAB | 1 | Intravenous (not otherwise specified) | 15 MG/KG OVER 30-90 MINUTES ON DAY 1 (STARTING WITH CYCLE 2). | Y | 125085 | 673 | MG | SOLUTION FOR INFUSION | ||||||
| 127980741 | 12798074 | 2 | SS | PACLITAXEL. | PACLITAXEL | 1 | Intravenous (not otherwise specified) | 175 MG/M2 OVER 3 HRS ON DAY 1 X 6 CYCLES | U | 0 | 175 | MG/M**2 | |||||||
| 127980741 | 12798074 | 3 | SS | CARBOPLATIN. | CARBOPLATIN | 1 | Intravenous (not otherwise specified) | CARBOPLATIN: AUC = 6 IV OVER 30 MINUTES ON DAY 1 X 6 CYCLES | U | 0 | |||||||||
| 127980741 | 12798074 | 4 | C | NEUPOGEN | FILGRASTIM | 1 | Unknown | 103353 | |||||||||||
| 127980741 | 12798074 | 5 | C | CEFTRIAXONE. | CEFTRIAXONE | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127980741 | 12798074 | 1 | Endometrial cancer |
| 127980741 | 12798074 | 2 | Endometrial cancer |
| 127980741 | 12798074 | 3 | Endometrial cancer |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127980741 | 12798074 | OT |
| 127980741 | 12798074 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127980741 | 12798074 | Acidosis | |
| 127980741 | 12798074 | Anaemia | |
| 127980741 | 12798074 | Dehydration | |
| 127980741 | 12798074 | Haemoglobin decreased | |
| 127980741 | 12798074 | Neutrophil count decreased | |
| 127980741 | 12798074 | Proteinuria | |
| 127980741 | 12798074 | White blood cell count decreased |
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 |
|---|---|---|---|---|---|---|
| 127980741 | 12798074 | 1 | 20100709 | 20121010 | 0 |