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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126800531 | 12680053 | 1 | I | 20160816 | 20160824 | 20160824 | EXP | US-AMGEN-USASP2016107548 | AMGEN | 0.00 | A | M | Y | 0.00000 | 20160824 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126800531 | 12680053 | 1 | PS | NEUPOGEN | FILGRASTIM | 1 | Unknown | 480 MUG, 3 TIMES/WK | 103353 | 480 | UG | SOLUTION FOR INJECTION | TIW | ||||||
| 126800531 | 12680053 | 2 | SS | NEUPOGEN | FILGRASTIM | 1 | Unknown | 480 MUG, 2 TIMES/WK | 103353 | 480 | UG | SOLUTION FOR INJECTION | BIW | ||||||
| 126800531 | 12680053 | 3 | C | METHOTREXATE. | METHOTREXATE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126800531 | 12680053 | 1 | Neutropenia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126800531 | 12680053 | DS |
| 126800531 | 12680053 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126800531 | 12680053 | Disability | |
| 126800531 | 12680053 | Expired product administered | |
| 126800531 | 12680053 | Intentional product misuse | |
| 126800531 | 12680053 | Laboratory test abnormal |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |