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
125080342 12508034 2 F 201605 20160615 20160629 20160721 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-38901BP BOEHRINGER INGELHEIM 56.27 YR F Y 0.00000 20160721 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
125080342 12508034 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 75 MG N 555982 20520 75 MG TABLET QD
125080342 12508034 2 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 75 MG N 555982 20520 75 MG TABLET QD
125080342 12508034 3 C ALEVE NAPROXEN SODIUM 1 Oral 0 TABLET
125080342 12508034 4 C EXCEDRIN ACETAMINOPHENASPIRINCAFFEINE 1 Oral 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125080342 12508034 1 Dyspepsia
125080342 12508034 3 Back pain
125080342 12508034 4 Headache

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125080342 12508034 Diarrhoea
125080342 12508034 Medication error
125080342 12508034 Vomiting

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
125080342 12508034 1 2011 20160611 0
125080342 12508034 2 201605 0
125080342 12508034 3 2011 0
125080342 12508034 4 2013 0