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
125710061 12571006 1 I 20160217 20160224 20160719 20160719 PER US-BAUSCH-BL-2016-004698 BAUSCH AND LOMB 50.41 YR F Y 69.46000 KG 20160719 MD 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
125710061 12571006 1 PS XIFAXAN RIFAXIMIN 1 Oral 21361 550 MG TABLET TID
125710061 12571006 2 SS IMODIUM LOPERAMIDE HYDROCHLORIDE 1 Unknown U 0
125710061 12571006 3 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 0 200 MG BID
125710061 12571006 4 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 0 40 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125710061 12571006 1 Irritable bowel syndrome
125710061 12571006 2 Diarrhoea
125710061 12571006 3 Product used for unknown indication
125710061 12571006 4 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125710061 12571006 Constipation
125710061 12571006 Diarrhoea

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
125710061 12571006 1 20160213 20160218 0
125710061 12571006 2 20160218 0
125710061 12571006 3 1987 0
125710061 12571006 4 2014 0