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
123149804 12314980 4 F 2011 20160726 20160428 20160728 EXP US-JNJFOC-20160417085 JANSSEN 0.00 A F Y 0.00000 20160728 CN US 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
123149804 12314980 1 SS STELARA USTEKINUMAB 1 Subcutaneous Y N UNKNOWN;UNKNOWN 0 SOLUTION FOR INJECTION
123149804 12314980 2 PS STELARA USTEKINUMAB 1 Subcutaneous Y N UNKNOWN;UNKNOWN 125261 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123149804 12314980 1 Psoriasis
123149804 12314980 2 Psoriasis

Outcome of event

Event ID CASEID OUTC COD
123149804 12314980 OT
123149804 12314980 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123149804 12314980 Drug effect decreased
123149804 12314980 Exposure during pregnancy
123149804 12314980 Psoriasis
123149804 12314980 Psoriatic arthropathy
123149804 12314980 Wound infection staphylococcal

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
123149804 12314980 1 2011 0