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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125637941 | 12563794 | 1 | I | 2016 | 20160712 | 20160716 | 20160716 | EXP | US-AMGEN-USASP2016090673 | AMGEN | 47.00 | YR | A | F | Y | 0.00000 | 20160716 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125637941 | 12563794 | 1 | PS | NEULASTA | PEGFILGRASTIM | 1 | Unknown | UNK | U | A40228-0006628 | 125031 | SOLUTION FOR INJECTION | |||||||
125637941 | 12563794 | 2 | SS | NEUPOGEN | FILGRASTIM | 1 | Unknown | 480 MG, QD (ONCE A DAY FOR 3 DAYS) | U | 0 | 480 | MG | UNKNOWN FORMULATION | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125637941 | 12563794 | 1 | Product used for unknown indication |
125637941 | 12563794 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125637941 | 12563794 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125637941 | 12563794 | Drug dose omission | |
125637941 | 12563794 | Neutrophil count abnormal | |
125637941 | 12563794 | 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 |
---|---|---|---|---|---|---|
125637941 | 12563794 | 2 | 20160623 | 20160627 | 0 |