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
126606372 12660637 2 F 20160607 20160610 20160817 20160901 EXP US-RELYPSA-RLY2016000997 RELYPSA 81.34 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
126606372 12660637 1 PS VELTASSA PATIROMER 1 Oral 8.4 G, QD Y VHCP 0 8.4 G ORAL SUSPENSION
126606372 12660637 2 SS CARVEDILOL. CARVEDILOL 1 6.25 MG, UNKNOWN 0 6.25 MG
126606372 12660637 3 SS LOSARTAN. LOSARTAN 1 100 MG, UNKNOWN 0 100 MG
126606372 12660637 4 SS AMLODIPINE AMLODIPINE BESYLATE 1 5 MG, UNKNOWN 0 5 MG
126606372 12660637 5 SS HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 25 MG, PRN 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126606372 12660637 1 Hyperkalaemia
126606372 12660637 5 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126606372 12660637 Blood pressure increased
126606372 12660637 Inhibitory drug interaction

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
126606372 12660637 1 20160607 20160609 0