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
126706362 12670636 2 F 20160811 20160822 20160822 PER PHEH2016US020437 NOVARTIS 0.00 M Y 0.00000 20160822 MD 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
126706362 12670636 1 PS ENTRESTO SACUBITRILVALSARTAN 1 Unknown 50 MG, BID U F0005 207620 50 MG BID
126706362 12670636 2 SS SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown 0
126706362 12670636 3 C LASIX FUROSEMIDE 1 Unknown U 0
126706362 12670636 4 C CARVEDILOL. CARVEDILOL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126706362 12670636 1 Product used for unknown indication
126706362 12670636 2 Product used for unknown indication
126706362 12670636 3 Product used for unknown indication
126706362 12670636 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126706362 12670636 Blood potassium increased
126706362 12670636 Blood urine present

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
126706362 12670636 1 20160714 0