The Safety Rates Drug Report

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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
126075451 12607545 1 I 2002 20160725 20160729 20160729 EXP PHHY2016BR103766 NOVARTIS 0.00 F Y 92.00000 KG 20160729 CN 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
126075451 12607545 1 PS DIOVAN VALSARTAN 1 Oral 1 DF, QD (DIOVAN 80 MG) 21283 1 DF TABLET QD
126075451 12607545 2 SS DIOVAN VALSARTAN 1 Oral 1 DF, QD (DIOVAN 160 MG) 21283 1 DF TABLET QD
126075451 12607545 3 SS DIOVAN HCT HYDROCHLOROTHIAZIDEVALSARTAN 1 Oral 1 DF, QD 0 1 DF TABLET QD
126075451 12607545 4 C AEROLIN ALBUTEROL 1 Unknown U 0
126075451 12607545 5 C HIDROMED HYDROCHLOROTHIAZIDE 1 Unknown U 0
126075451 12607545 6 C AMLODIPINO//AMLODIPINE 2 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126075451 12607545 1 Hypertension
126075451 12607545 3 Hypertension
126075451 12607545 4 Product used for unknown indication
126075451 12607545 5 Product used for unknown indication
126075451 12607545 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126075451 12607545 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126075451 12607545 Diabetes mellitus

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
126075451 12607545 1 2002 0