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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120947512 | 12094751 | 2 | F | 20140528 | 20160808 | 20160219 | 20160816 | EXP | DE-SA-2016SA029601 | AVENTIS | 72.00 | YR | E | M | Y | 90.00000 | KG | 20160816 | MD | DE | DE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120947512 | 12094751 | 1 | PS | DOCETAXEL. | DOCETAXEL | 1 | Intravenous (not otherwise specified) | UNKNOWN | 20449 | 110 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | /cycle |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
120947512 | 12094751 | 1 | Prostate cancer |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
120947512 | 12094751 | OT |
120947512 | 12094751 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
120947512 | 12094751 | Activities of daily living impaired | |
120947512 | 12094751 | Dyspnoea | |
120947512 | 12094751 | Fatigue | |
120947512 | 12094751 | Mucosal infection |
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 |
---|---|---|---|---|---|---|
120947512 | 12094751 | 1 | 20140416 | 20140910 | 0 |