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
125704412 12570441 2 F 20160613 20160713 20160719 20160901 EXP US-RELYPSA-RLY2016001122 RELYPSA 68.29 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
125704412 12570441 1 PS VELTASSA PATIROMER 1 Oral 16.8 G, QD VEXMA 0 16.8 G ORAL SUSPENSION
125704412 12570441 2 SS SODIUM BICARBONATE. SODIUM BICARBONATE 1 Unknown U U UNKNOWN 0
125704412 12570441 3 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0
125704412 12570441 4 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 0
125704412 12570441 5 C CHLORTHALIDONE. CHLORTHALIDONE 1 0
125704412 12570441 6 C VITAMIN D /00107901/ ERGOCALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125704412 12570441 1 Hyperkalaemia
125704412 12570441 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125704412 12570441 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125704412 12570441 Gastrointestinal haemorrhage
125704412 12570441 Haemorrhagic anaemia
125704412 12570441 Melaena
125704412 12570441 Nausea

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
125704412 12570441 1 20160121 0