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
125587671 12558767 1 I 20120604 20160715 20160715 PER US-JNJFOC-20120602164 JANSSEN 63.00 YR A F Y 58.06000 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
125587671 12558767 1 PS IMODIUM MULTI-SYMPTOM RELIEF DIMETHICONELOPERAMIDE HYDROCHLORIDE 1 Oral Y U CHF018;CHF018;CHF018 20606 CHEWABLE TABLET
125587671 12558767 2 SS IMODIUM MULTI-SYMPTOM RELIEF DIMETHICONELOPERAMIDE HYDROCHLORIDE 1 Oral Y U CHF018;CHF018;CHF018 20606 CHEWABLE TABLET
125587671 12558767 3 SS IMODIUM A-D LOPERAMIDE HYDROCHLORIDE 1 Oral Y U CHF018 19487 LIQUID
125587671 12558767 4 SS IMODIUM A-D LOPERAMIDE HYDROCHLORIDE 1 Oral Y U CHF018 19487 LIQUID
125587671 12558767 5 C LOMOTIL ATROPINE SULFATEDIPHENOXYLATE HYDROCHLORIDE 1 Unknown 0 UNSPECIFIED
125587671 12558767 6 C LORAZEPAM. LORAZEPAM 1 Unknown 0 UNSPECIFIED
125587671 12558767 7 C PHENERGAN PROMETHAZINE HYDROCHLORIDE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125587671 12558767 2 Diarrhoea
125587671 12558767 3 Vomiting
125587671 12558767 4 Diarrhoea
125587671 12558767 5 Ulcer haemorrhage
125587671 12558767 6 Anxiety
125587671 12558767 7 Nausea

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125587671 12558767 Drug ineffective
125587671 12558767 Poor quality drug administered
125587671 12558767 Product taste abnormal
125587671 12558767 Retching

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

no results found

Therapies reported

no results found