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
127374001 12737400 1 I 20160821 20160905 20160912 20160912 EXP PHHY2016BR125219 NOVARTIS 79.77 YR F Y 65.00000 KG 20160912 OT 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
127374001 12737400 1 PS DIOVAN HCT HYDROCHLOROTHIAZIDEVALSARTAN 1 Unknown 1 DF (HYDROCHLOROTHIAZIDE UNK, VALSARTAN 80 MG, UNK 20818 1 DF TABLET QD
127374001 12737400 2 SS DIOVAN HCT HYDROCHLOROTHIAZIDEVALSARTAN 1 Oral 1 DF(HYDROCHLOROTHIAZIDE 25 MG, VALSARTAN320 MG), QD 20818 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127374001 12737400 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127374001 12737400 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127374001 12737400 Cough
127374001 12737400 Drug dispensing error
127374001 12737400 Fear
127374001 12737400 Leukocytosis
127374001 12737400 Malaise
127374001 12737400 Pneumonia

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
127374001 12737400 1 19960606 0