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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127010411 | 12701041 | 1 | I | 20160813 | 0 | 20160830 | 20160830 | DIR | 78.29 | YR | M | N | 62.10000 | KG | 20160829 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127010411 | 12701041 | 1 | PS | CASODEX | BICALUTAMIDE | 1 | 0 | 9000 | MG | ||||||||||
127010411 | 12701041 | 2 | SS | LEUPROLIDE ACETATE. | LEUPROLIDE ACETATE | 1 | D | D | 0 | 45 | MG |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127010411 | 12701041 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127010411 | 12701041 | Abdominal pain | |
127010411 | 12701041 | Bladder disorder | |
127010411 | 12701041 | Diarrhoea | |
127010411 | 12701041 | Faeces discoloured | |
127010411 | 12701041 | Gastrointestinal wall thickening | |
127010411 | 12701041 | Rectal haemorrhage |
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 |
---|---|---|---|---|---|---|
127010411 | 12701041 | 1 | 20160504 | 0 | ||
127010411 | 12701041 | 2 | 20160208 | 0 |