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
125269831 12526983 1 I 20160620 20160705 20160705 EXP US-GLAXOSMITHKLINE-US2016GSK088540 GLAXOSMITHKLINE 0.00 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
125269831 12526983 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 U 18703
125269831 12526983 2 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 U 18703
125269831 12526983 3 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 U 18703
125269831 12526983 4 SS GAVISCON ALUMINUM HYDROXIDEMAGNESIUM CARBONATE 1 U 0
125269831 12526983 5 SS GAVISCON ALUMINUM HYDROXIDEMAGNESIUM CARBONATE 1 U 0
125269831 12526983 6 SS GAVISCON ALUMINUM HYDROXIDEMAGNESIUM CARBONATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125269831 12526983 1 Abdominal pain upper
125269831 12526983 2 Abdominal discomfort
125269831 12526983 3 Nausea
125269831 12526983 4 Abdominal pain upper
125269831 12526983 5 Abdominal discomfort
125269831 12526983 6 Nausea

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125269831 12526983 Drug ineffective

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

no results found

Therapies reported

no results found