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
126075301 12607530 1 I 20160723 20160729 20160729 EXP PHHY2016BR103229 NOVARTIS 0.00 M Y 78.00000 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
126075301 12607530 1 PS DIOVAN HCT HYDROCHLOROTHIAZIDEVALSARTAN 1 Unknown 1 DF (HYDROCHLOROTHIAZIDE 12.5 MG, VALSARTAN 160MG) Y 20818 1 DF TABLET
126075301 12607530 2 SS DIOVAN VALSARTAN 1 Oral 160 MG, BID Y 0 160 MG TABLET BID
126075301 12607530 3 SS DIOVAN VALSARTAN 1 Oral 320 MG, BID Y 0 320 MG TABLET BID
126075301 12607530 4 SS DIOVAN VALSARTAN 1 Oral 1 DF (12.5 MG), BID Y 0 1 DF TABLET BID
126075301 12607530 5 C HYDROCORTISONE. HYDROCORTISONE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126075301 12607530 1 Hypertension
126075301 12607530 2 Hypertension
126075301 12607530 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126075301 12607530 HO
126075301 12607530 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126075301 12607530 Arrhythmia
126075301 12607530 Arterial occlusive disease
126075301 12607530 Blood pressure fluctuation
126075301 12607530 Blood pressure increased
126075301 12607530 Drug ineffective
126075301 12607530 Fall
126075301 12607530 Hyperhidrosis
126075301 12607530 Malaise
126075301 12607530 Polyuria
126075301 12607530 Syncope
126075301 12607530 Upper limb 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
126075301 12607530 2 2016 0