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
127092482 12709248 2 F 201607 20160924 20160901 20160928 EXP US-BAUSCH-BL-2016-020850 BAUSCH AND LOMB 56.47 YR F Y 0.00000 20160928 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
127092482 12709248 1 PS XIFAXAN RIFAXIMIN 1 Unknown U SCKD 21361 550 MG TABLET BID
127092482 12709248 2 SS XIFAXAN RIFAXIMIN 1 U SCKD 21361
127092482 12709248 3 SS LACTULOSE. LACTULOSE 1 Unknown U 0 60 MG QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127092482 12709248 1 Hepatic encephalopathy
127092482 12709248 2 Chronic hepatic failure
127092482 12709248 3 Chronic hepatic failure

Outcome of event

Event ID CASEID OUTC COD
127092482 12709248 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127092482 12709248 Ammonia increased
127092482 12709248 Blood count abnormal
127092482 12709248 Confusional state
127092482 12709248 Constipation
127092482 12709248 Gastrointestinal motility disorder

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

no results found

Therapies reported

no results found