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
124659522 12465952 2 F 201604 20160531 20160614 20160721 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-35212BP BOEHRINGER INGELHEIM 72.17 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
124659522 12465952 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 50 MG Y 654529A 21698 150 MG TABLET
124659522 12465952 2 SS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 3 ANZ Y 654529A 21698 TABLET QD
124659522 12465952 3 C TAMOXIFEN TAMOXIFEN 1 Oral 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124659522 12465952 1 Dyspepsia
124659522 12465952 2 Dyspepsia
124659522 12465952 3 Breast cancer

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124659522 12465952 Drug ineffective
124659522 12465952 Incorrect drug administration duration
124659522 12465952 Medication error

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
124659522 12465952 1 201604 201605 0
124659522 12465952 3 201602 0