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
125587341 12558734 1 I 20160613 20160715 20160715 PER US-JNJFOC-20160612805 JANSSEN 67.00 YR E F Y 100.70000 KG 20160715 CN US US

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
125587341 12558734 1 PS IMODIUM MULTI-SYMPTOM RELIEF DIMETHICONELOPERAMIDE HYDROCHLORIDE 1 Oral U U HSF061 21140 CAPLET
125587341 12558734 2 SS IMODIUM MULTI-SYMPTOM RELIEF DIMETHICONELOPERAMIDE HYDROCHLORIDE 1 Oral U U HSF061 21140 CAPLET
125587341 12558734 3 C NORVASC AMLODIPINE BESYLATE 1 Unknown 0 30 MG UNSPECIFIED TID
125587341 12558734 4 C ASPIRIN. ASPIRIN 1 Unknown 0 UNSPECIFIED
125587341 12558734 5 C LOSARTAN. LOSARTAN 1 Unknown 0 100 MG UNSPECIFIED QD
125587341 12558734 6 C VESICARE SOLIFENACIN SUCCINATE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125587341 12558734 1 Irritable bowel syndrome
125587341 12558734 2 Diarrhoea
125587341 12558734 3 Hypertension
125587341 12558734 4 Cardiac disorder
125587341 12558734 5 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125587341 12558734 Drug ineffective for unapproved indication
125587341 12558734 Off label use
125587341 12558734 Product use issue

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
125587341 12558734 1 20160612 20160613 0
125587341 12558734 2 20160612 20160613 0