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
127669041 12766904 1 I 200409 20160912 20160921 20160921 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-59975BP BOEHRINGER INGELHEIM 45.46 YR M Y 0.00000 20160921 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
127669041 12766904 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 300 MG 20520 150 MG TABLET
127669041 12766904 2 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 75 MG 20520 75 MG TABLET
127669041 12766904 3 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 75 MG 20520 75 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127669041 12766904 1 Dyspepsia
127669041 12766904 2 Gallbladder disorder

Outcome of event

Event ID CASEID OUTC COD
127669041 12766904 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127669041 12766904 Abdominal pain upper
127669041 12766904 Cholelithiasis
127669041 12766904 Dyspepsia
127669041 12766904 Fall
127669041 12766904 Food intolerance
127669041 12766904 Gallbladder disorder
127669041 12766904 Gallbladder pain
127669041 12766904 Incorrect drug administration duration
127669041 12766904 Off label use

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
127669041 12766904 1 20160911 20160912 0
127669041 12766904 2 20160912 0
127669041 12766904 3 200409 200505 0