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
124810463 12481046 3 F 20160519 20160818 20160620 20160826 EXP DE-ABBVIE-16K-062-1651014-00 ABBVIE 55.07 YR F Y 82.00000 KG 20160826 MD 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
124810463 12481046 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
124810463 12481046 2 SS SIMVASTATIN. SIMVASTATIN 1 Unknown Y UNKNOWN 0
124810463 12481046 3 C MARCUMAR PHENPROCOUMON 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124810463 12481046 1 Crohn's disease
124810463 12481046 2 Product used for unknown indication
124810463 12481046 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124810463 12481046 OT
124810463 12481046 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124810463 12481046 Blood creatine phosphokinase increased
124810463 12481046 Bronchitis
124810463 12481046 Choking
124810463 12481046 Muscle atrophy
124810463 12481046 Myocarditis
124810463 12481046 Nasopharyngitis

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
124810463 12481046 1 20121210 20160523 0
124810463 12481046 2 201605 0