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
124822933 12482293 3 F 201602 20160714 20160620 20160715 EXP GB-JNJFOC-20160515808 JANSSEN 46.69 YR A M Y 87.00000 KG 20160715 MD GB GB

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
124822933 12482293 1 SS STELARA USTEKINUMAB 1 Subcutaneous N U FE50MD 0 45 MG SOLUTION FOR INJECTION
124822933 12482293 2 PS STELARA USTEKINUMAB 1 Subcutaneous N U FE50MD 125261 45 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124822933 12482293 1 Pustular psoriasis
124822933 12482293 2 Psoriasis

Outcome of event

Event ID CASEID OUTC COD
124822933 12482293 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124822933 12482293 Asthenia
124822933 12482293 Chills
124822933 12482293 Night sweats
124822933 12482293 Off label use
124822933 12482293 Product use issue
124822933 12482293 Psoriasis
124822933 12482293 Psoriatic arthropathy
124822933 12482293 Pustular psoriasis
124822933 12482293 Temperature regulation disorder

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
124822933 12482293 1 201602 0
124822933 12482293 2 201602 0