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
126578492 12657849 2 F 20160812 20160817 20160819 PER PHEH2016US020539 NOVARTIS 0.00 Y 0.00000 20160819 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
126578492 12657849 1 PS COSENTYX SECUKINUMAB 1 Subcutaneous 150 MG, QMO U 125504 150 MG INJECTION /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126578492 12657849 1 Psoriatic arthropathy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126578492 12657849 Nasopharyngitis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found