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
124853032 12485303 2 F 20160501 20160628 20160621 20160706 EXP PHHY2016AR066914 NOVARTIS 65.43 YR F Y 0.00000 20160706 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
124853032 12485303 1 PS DIOVAN VALSARTAN 1 Unknown 2 DF (80, UNITS NOT PROVIDED), QD Y U 21283 2 DF TABLET QD
124853032 12485303 2 SS DIOVAN VALSARTAN 1 Unknown 2 DF (160, UNITS NOT PROVIDED), QD Y U 21283 2 DF TABLET QD
124853032 12485303 3 SS DIOVAN VALSARTAN 1 Unknown 1 DF (320, UNITS NOT PROVIDED), QD (SIX MONTHS AGO) Y U B8055A 21283 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124853032 12485303 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
124853032 12485303 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124853032 12485303 Blood pressure increased
124853032 12485303 Drug ineffective
124853032 12485303 Fall
124853032 12485303 Hypotension
124853032 12485303 Spinal fracture

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
124853032 12485303 1 2013 0
124853032 12485303 3 201605 0