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
126028782 12602878 2 F 201607 20160722 20160728 20160729 EXP PHHY2016BR102560 NOVARTIS 79.46 YR M Y 97.00000 KG 20160729 MD BR BR

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
126028782 12602878 1 PS DIOVAN VALSARTAN 1 Oral 1 DF, QD (320 MG) Y 21283 1 DF TABLET QD
126028782 12602878 2 SS DIOVAN VALSARTAN 1 Oral 1 DF, QD (160 MG) Y 21283 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126028782 12602878 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126028782 12602878 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126028782 12602878 Burning sensation
126028782 12602878 Cardiac disorder
126028782 12602878 Dizziness
126028782 12602878 Drug ineffective
126028782 12602878 Dyspnoea
126028782 12602878 Fatigue
126028782 12602878 Hernia pain
126028782 12602878 Influenza
126028782 12602878 Inguinal hernia
126028782 12602878 Lung cyst
126028782 12602878 Malaise
126028782 12602878 Nasopharyngitis

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
126028782 12602878 1 2012 0
126028782 12602878 2 20160222 201603 0