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
125581061 12558106 1 I 201512 20160706 20160714 20160714 EXP CA-ABBVIE-16K-028-1672371-00 ABBVIE 70.34 YR F Y 0.00000 20160714 CN COUNTRY NOT SPECIFIED CA

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
125581061 12558106 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW
125581061 12558106 2 SS CEPHALEXIN. CEPHALEXIN 1 Intravenous (not otherwise specified) UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125581061 12558106 1 Psoriatic arthropathy
125581061 12558106 2 Infection

Outcome of event

Event ID CASEID OUTC COD
125581061 12558106 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125581061 12558106 Arthritis
125581061 12558106 Calcinosis
125581061 12558106 Clostridium difficile infection
125581061 12558106 Hypophagia
125581061 12558106 Infection
125581061 12558106 Malaise
125581061 12558106 Secretion discharge
125581061 12558106 Weight decreased
125581061 12558106 Wound secretion

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
125581061 12558106 1 20130528 201601 0
125581061 12558106 2 2016 2016 0