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
125595801 12559580 1 I 20160711 20160715 20160715 EXP PHHY2016AR096430 NOVARTIS 0.00 F Y 0.00000 20160715 CN COUNTRY NOT SPECIFIED AR

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
125595801 12559580 1 PS DIOVAN VALSARTAN 1 Unknown 0.5 DF (160 UNITS NOT PROVIDED), BID (HALF AT NIGHT AND HALF IN THE MORNING) U 20665 .5 DF BID
125595801 12559580 2 SS DIOVAN VALSARTAN 1 Unknown 160 OT, (SOME DAYS AGO) U 20665

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125595801 12559580 1 Hypertension
125595801 12559580 2 Arrhythmia

Outcome of event

Event ID CASEID OUTC COD
125595801 12559580 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125595801 12559580 Arrhythmia
125595801 12559580 Influenza
125595801 12559580 Wrong technique in product usage process

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found