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
117337352 11733735 2 F 201509 20160707 20151113 20160714 EXP IT-ABBVIE-15K-083-1496488-00 ABBVIE 75.45 YR F Y 0.00000 20160714 MD IT IT

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
117337352 11733735 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
117337352 11733735 1 Psoriasis

Outcome of event

Event ID CASEID OUTC COD
117337352 11733735 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
117337352 11733735 Erythrodermic psoriasis
117337352 11733735 Neutrophil count increased
117337352 11733735 Pleural effusion
117337352 11733735 Psoriasis
117337352 11733735 Pustular psoriasis
117337352 11733735 Skin infection
117337352 11733735 Skin lesion
117337352 11733735 White blood cell count increased

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
117337352 11733735 1 20130408 20151017 0