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
127641232 12764123 2 F 201609 20160929 20160920 20160929 EXP US-BAUSCH-BL-2016-022941 BAUSCH AND LOMB 67.95 YR F Y 0.00000 20160929 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
127641232 12764123 1 PS XIFAXAN RIFAXIMIN 1 Oral D SMTC 21361 TABLET BID
127641232 12764123 2 SS LACTULOSE. LACTULOSE 1 Oral 10-15 ML D 0 LIQUID BID
127641232 12764123 3 SS LACTULOSE. LACTULOSE 1 Oral 10-15 ML D 0 LIQUID TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127641232 12764123 1 Liver disorder
127641232 12764123 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127641232 12764123 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127641232 12764123 Ammonia increased
127641232 12764123 Drug dose omission
127641232 12764123 Feeling abnormal
127641232 12764123 Headache
127641232 12764123 Somnolence

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
127641232 12764123 1 201608 0