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
108890554 10889055 4 F 2013 20160913 20150305 20160915 EXP AR-ABBVIE-15K-007-1344032-00 ABBVIE 0.00 F Y 0.00000 20160915 CN COUNTRY NOT SPECIFIED AR

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
108890554 10889055 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108890554 10889055 1 Psoriatic arthropathy

Outcome of event

Event ID CASEID OUTC COD
108890554 10889055 DS
108890554 10889055 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108890554 10889055 Accident
108890554 10889055 Fall
108890554 10889055 Furuncle
108890554 10889055 Haemarthrosis
108890554 10889055 Joint effusion
108890554 10889055 Joint injury
108890554 10889055 Joint stiffness
108890554 10889055 Osteoarthritis
108890554 10889055 Peripheral nerve injury
108890554 10889055 Psoriatic arthropathy
108890554 10889055 Tendon rupture

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
108890554 10889055 1 20120913 0