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
124305432 12430543 2 F 2001 20160620 20160602 20160705 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-31791BP BOEHRINGER INGELHEIM 67.48 YR F Y 0.00000 20160705 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
124305432 12430543 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 75 MG 559986 20520 75 MG TABLET QD
124305432 12430543 2 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 Unknown 75 MG 559986 20520 75 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124305432 12430543 1 Gastrooesophageal reflux disease
124305432 12430543 2 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124305432 12430543 Abdominal pain upper
124305432 12430543 Diarrhoea
124305432 12430543 Eructation
124305432 12430543 Feeling abnormal
124305432 12430543 Gastrooesophageal reflux disease
124305432 12430543 Incorrect dosage administered
124305432 12430543 Malaise
124305432 12430543 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
124305432 12430543 1 2001 0