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
127070292 12707029 2 F 201607 20160908 20160901 20160915 EXP PHHY2016MX119124 NOVARTIS 58.03 YR F Y 54.00000 KG 20160915 CN COUNTRY NOT SPECIFIED MX

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
127070292 12707029 1 PS RASILEZ HCT ALISKIRENHYDROCHLOROTHIAZIDE 1 Oral 1 DF, QD (ALISKIREN 300 MG AND HYDROCHLOROTHIAZIDE 12.5 MG) (APPROXIMATELY IN 2011, 5 YEARS AGO) U T3180 22107 1 DF TABLET QD
127070292 12707029 2 SS RASILEZ ALISKIREN 1 Oral 1 DF, QD 0 1 DF TABLET QD
127070292 12707029 3 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Oral 0.5 DF (25 MG) 0 .5 DF TABLET
127070292 12707029 4 C ILTUX HCT 2 Oral 1 DF, QD (ONLY FOR 14 DAYS) Y 0 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127070292 12707029 1 Hypertension
127070292 12707029 2 Hypertension
127070292 12707029 3 Hypertension
127070292 12707029 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127070292 12707029 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127070292 12707029 Blood pressure increased

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
127070292 12707029 3 201602 0
127070292 12707029 4 201602 201602 0