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
125448121 12544812 1 I 20160627 20160627 20160711 20160711 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-41777BP BOEHRINGER INGELHEIM 79.77 YR F Y 0.00000 20160711 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
125448121 12544812 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 560385 20520 150 MG TABLET
125448121 12544812 2 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 0.75 MG 0 .75 MG TABLET QD
125448121 12544812 3 C LIPITOR ATORVASTATIN CALCIUM 1 Oral 40 MG 0 40 MG TABLET QD
125448121 12544812 4 C FOLIC ACID. FOLIC ACID 1 Oral 1 MG 0 1 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125448121 12544812 1 Dyspepsia
125448121 12544812 2 Hypothyroidism
125448121 12544812 3 Blood cholesterol increased
125448121 12544812 4 Supplementation therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125448121 12544812 Back pain
125448121 12544812 Chest pain

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
125448121 12544812 1 20160627 0
125448121 12544812 2 1996 0
125448121 12544812 3 1996 0
125448121 12544812 4 1996 0