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
127658951 12765895 1 I 201510 20160914 20160921 20160921 EXP PHHY2016VE128278 NOVARTIS 65.13 YR F Y 0.00000 20160921 CN COUNTRY NOT SPECIFIED VE

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
127658951 12765895 1 PS DIOVAN VALSARTAN 1 Oral 40 MG, QD U 20665 40 MG QD
127658951 12765895 2 SS DIOVAN VALSARTAN 1 Unknown 80 MG, UNK U 20665 80 MG
127658951 12765895 3 SS VALSARTAN. VALSARTAN 1 Unknown U 20665
127658951 12765895 4 SS BIOTALOL BISOPROLOL FUMARATE 1 Unknown UNK U 0
127658951 12765895 5 SS BIOTALOL BISOPROLOL FUMARATE 1 Unknown 0.5 DF, UNK U 0 .5 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127658951 12765895 1 Hypertension
127658951 12765895 3 Hypertension
127658951 12765895 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127658951 12765895 OT
127658951 12765895 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127658951 12765895 Breast cancer
127658951 12765895 Hypotension
127658951 12765895 Seizure
127658951 12765895 Underdose

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
127658951 12765895 1 2007 0