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
125223801 12522380 1 I 201512 20160623 20160701 20160701 EXP US-ABBVIE-16K-163-1660489-00 ABBVIE 44.19 YR F Y 0.00000 20160701 CN COUNTRY NOT SPECIFIED 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
125223801 12522380 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
125223801 12522380 2 SS SULFASALAZINE. SULFASALAZINE 1 Unknown U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125223801 12522380 1 Psoriatic arthropathy
125223801 12522380 2 Eye disorder

Outcome of event

Event ID CASEID OUTC COD
125223801 12522380 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125223801 12522380 Abdominal discomfort
125223801 12522380 Arthropathy
125223801 12522380 Eye disorder
125223801 12522380 Fatigue
125223801 12522380 Inflammation
125223801 12522380 Rash macular
125223801 12522380 Skin exfoliation
125223801 12522380 Skin irritation

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
125223801 12522380 1 201303 0
125223801 12522380 2 2016 0