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
111867582 11186758 2 F 201409 20160818 20150613 20160826 EXP DE-ABBVIE-15K-062-1407174-00 ABBVIE 5.90 MON F Y 0.00000 20160826 CN COUNTRY NOT SPECIFIED DE

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
111867582 11186758 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous N UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
111867582 11186758 2 C METOHEXAL METOPROLOL SUCCINATE 1 0
111867582 11186758 3 C MAPROTILIN MAPROTILINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111867582 11186758 1 Rheumatoid arthritis
111867582 11186758 2 Product used for unknown indication
111867582 11186758 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
111867582 11186758 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
111867582 11186758 Back pain
111867582 11186758 Intervertebral disc protrusion
111867582 11186758 Pain in extremity

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
111867582 11186758 1 20140714 201412 0