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
127878171 12787817 1 I 20160922 20160928 20160928 EXP PHHY2016BR132661 NOVARTIS 80.00 YR F Y 72.00000 KG 20160928 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
127878171 12787817 1 PS DIOVAN HCT HYDROCHLOROTHIAZIDEVALSARTAN 1 Oral 1 DF (HYDROCHLOROTHIAZIDE 25 MG, VALSARTAN 160 MG) + 10 MG, QD U 20818 1 DF TABLET QD
127878171 12787817 2 C VITAMIN D CHOLECALCIFEROL 1 Oral 18 DRP, EVERY WEEK 0 18 GTT SOLUTION
127878171 12787817 3 C CALTRATE CALCIUM CARBONATE 1 Oral 2 DF, QD 0 2 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127878171 12787817 1 Hypertension
127878171 12787817 2 Osteoporosis
127878171 12787817 3 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
127878171 12787817 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127878171 12787817 Arthralgia
127878171 12787817 Body height decreased
127878171 12787817 Feeling abnormal
127878171 12787817 Hip fracture
127878171 12787817 Malaise
127878171 12787817 Memory impairment

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

no results found

Therapies reported

no results found