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
126029541 12602954 1 I 20160720 20160728 20160728 EXP PHHY2016BR101526 NOVARTIS 0.00 F Y 76.00000 KG 20160728 MD COUNTRY NOT SPECIFIED 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
126029541 12602954 1 PS DIOVAN VALSARTAN 1 Unknown U 20665
126029541 12602954 2 SS OPTI FREE PANCRELIPASETYROSINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126029541 12602954 1 Hypertension
126029541 12602954 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126029541 12602954 HO
126029541 12602954 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126029541 12602954 Hypoacusis
126029541 12602954 Labyrinthitis
126029541 12602954 Malaise

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

no results found

Therapies reported

no results found