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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123601633 | 12360163 | 3 | F | 20160419 | 20160715 | 20160512 | 20160901 | EXP | US-RELYPSA-RLY2016000549 | RELYPSA | 72.44 | YR | F | Y | 0.00000 | 20160901 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123601633 | 12360163 | 1 | PS | VELTASSA | PATIROMER | 1 | Oral | 8.4 G, QD | 403.200012 | G | Y | UNKNOWN | 0 | 8.4 | G | ORAL SUSPENSION | |||
123601633 | 12360163 | 2 | SS | WELCHOL | COLESEVELAM HYDROCHLORIDE | 1 | Unknown | UNK | Y | U | UNKNOWN | 0 | |||||||
123601633 | 12360163 | 3 | SS | WELCHOL | COLESEVELAM HYDROCHLORIDE | 1 | Unknown | UNK | Y | U | UNKNOWN | 0 | |||||||
123601633 | 12360163 | 4 | C | DIOVAN | VALSARTAN | 1 | 0 | ||||||||||||
123601633 | 12360163 | 5 | C | AMLODIPINE BESYLATE. | AMLODIPINE BESYLATE | 1 | 0 | ||||||||||||
123601633 | 12360163 | 6 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | 0 | ||||||||||||
123601633 | 12360163 | 7 | C | BYSTOLIC | NEBIVOLOL HYDROCHLORIDE | 1 | 0 | ||||||||||||
123601633 | 12360163 | 8 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | 0 | ||||||||||||
123601633 | 12360163 | 9 | C | XARELTO | RIVAROXABAN | 1 | 0 | ||||||||||||
123601633 | 12360163 | 10 | C | DULOXETINE HCL | DULOXETINE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123601633 | 12360163 | 1 | Hyperkalaemia |
123601633 | 12360163 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
123601633 | 12360163 | OT |
123601633 | 12360163 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123601633 | 12360163 | Constipation |
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 |
---|---|---|---|---|---|---|
123601633 | 12360163 | 1 | 20160303 | 20160421 | 0 | |
123601633 | 12360163 | 2 | 20160421 | 0 | ||
123601633 | 12360163 | 3 | 2016 | 0 |