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
126861531 12686153 1 I 20160807 20160815 20160825 20160825 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-53610BP BOEHRINGER INGELHEIM 80.80 YR F Y 0.00000 20160825 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
126861531 12686153 1 PS ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 150 MG 560605 21698 150 MG TABLET QD
126861531 12686153 2 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 25 MCG 0 25 UG TABLET QD
126861531 12686153 3 C HUMIRA ADALIMUMAB 1 Subcutaneous 2.6667 MG 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126861531 12686153 1 Gastrooesophageal reflux disease
126861531 12686153 2 Hypothyroidism
126861531 12686153 3 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126861531 12686153 Nausea
126861531 12686153 Off label use

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
126861531 12686153 1 20160807 0
126861531 12686153 2 2011 0
126861531 12686153 3 2011 0