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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127264331 | 12726433 | 1 | I | 20151107 | 20160825 | 20160908 | 20160908 | EXP | PA20150795 | FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002576 | VALIDUS | 83.00 | YR | M | Y | 0.00000 | 20160908 | OT | FR | FR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127264331 | 12726433 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | UNK, TID | Y | 16273 | |||||||||
127264331 | 12726433 | 2 | SS | COLCHIMAX /01722001/ | COLCHICINEOPIUMTIEMONIUM METHYLSULFATE | 1 | Oral | UNK, TID | Y | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127264331 | 12726433 | 1 | Cardiac failure |
127264331 | 12726433 | 2 | Gout |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127264331 | 12726433 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127264331 | 12726433 | Acute kidney injury | |
127264331 | 12726433 | Dehydration | |
127264331 | 12726433 | Diarrhoea | |
127264331 | 12726433 | Hypokalaemia | |
127264331 | 12726433 | Vomiting |
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 |
---|---|---|---|---|---|---|
127264331 | 12726433 | 1 | 20151030 | 20151107 | 0 | |
127264331 | 12726433 | 2 | 20151030 | 20151107 | 0 |