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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125557991 | 12555799 | 1 | I | 20160622 | 0 | 20160713 | 20160713 | DIR | 60.39 | YR | F | N | 172.50000 | KG | 20160707 | N | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125557991 | 12555799 | 1 | PS | DOXIL | DOXORUBICIN HYDROCHLORIDE | 1 | D | D | 0 | 80 | MG |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125557991 | 12555799 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125557991 | 12555799 | Confusional state | |
125557991 | 12555799 | Dehydration | |
125557991 | 12555799 | Dizziness | |
125557991 | 12555799 | Fatigue | |
125557991 | 12555799 | Lumbar spinal stenosis | |
125557991 | 12555799 | Nausea | |
125557991 | 12555799 | Spondylolisthesis |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | CASEID | RPSR COD |
---|---|---|
125557991 | 12555799 | HP |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125557991 | 12555799 | 1 | 20160616 | 0 |