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
117917652 11791765 2 F 20160718 20151201 20160722 EXP PHHY2015BR157293 NOVARTIS 84.00 YR F Y 0.00000 20160722 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
117917652 11791765 1 PS RASILEZ HCT ALISKIRENHYDROCHLOROTHIAZIDE 1 Unknown 22107 TABLET
117917652 11791765 2 SS EXFORGE HCT AMLODIPINE BESYLATEHYDROCHLOROTHIAZIDEVALSARTAN 1 Unknown 0
117917652 11791765 3 SS DIOVAN VALSARTAN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117917652 11791765 1 Product used for unknown indication
117917652 11791765 2 Product used for unknown indication
117917652 11791765 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117917652 11791765 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117917652 11791765 Arrhythmia
117917652 11791765 Depressed mood
117917652 11791765 Drug intolerance
117917652 11791765 Heart rate increased
117917652 11791765 Hypoacusis
117917652 11791765 Malaise
117917652 11791765 Myringitis
117917652 11791765 Palpitations
117917652 11791765 Peripheral swelling

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

no results found

Therapies reported

no results found