The Safety Rates Drug Report

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Drug     Injury     Quarter    

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