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
124432883 12443288 3 F 201502 20160719 20160607 20160803 EXP US-GLAXOSMITHKLINE-US2016GSK073305 GLAXOSMITHKLINE 70.60 YR M Y 0.00000 20160803 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
124432883 12443288 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 300 MG, BID U 18703 300 MG BID
124432883 12443288 2 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 75 MG, BID U 18703 75 MG BID
124432883 12443288 3 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 150 MG, BID U 18703 150 MG BID
124432883 12443288 4 SS RANITIDINE HYDROCHLORIDE. RANITIDINE HYDROCHLORIDE 1 300 MG, BID U 18703 300 MG BID
124432883 12443288 5 C SUTENT SUNITINIB MALATE 1 0
124432883 12443288 6 C VITAMIN B12 CYANOCOBALAMIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124432883 12443288 1 Dyspepsia
124432883 12443288 2 Dyspepsia
124432883 12443288 4 Dyspepsia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124432883 12443288 Decreased appetite
124432883 12443288 Drug ineffective
124432883 12443288 Oral pain
124432883 12443288 Pruritus

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

no results found

Therapies reported

no results found