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
108460045 10846004 5 F 201405 20160718 20150220 20160726 EXP US-ABBVIE-15K-163-1329054-00 ABBVIE 72.50 YR F Y 0.00000 20160726 MD 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
108460045 10846004 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous U UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
108460045 10846004 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous U UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
108460045 10846004 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous U UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN QOW
108460045 10846004 4 C FUROSEMIDE. FUROSEMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108460045 10846004 1 Crohn's disease
108460045 10846004 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
108460045 10846004 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
108460045 10846004 Abdominal pain
108460045 10846004 Arthralgia
108460045 10846004 Candida infection
108460045 10846004 Dysphonia
108460045 10846004 Escherichia urinary tract infection
108460045 10846004 Fatigue
108460045 10846004 Flank pain
108460045 10846004 Hallucination, visual
108460045 10846004 Laryngitis
108460045 10846004 Pneumonia

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
108460045 10846004 1 20121201 20140225 0
108460045 10846004 2 20140225 201405 0
108460045 10846004 3 201505 0