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
126019832 12601983 2 F 201607 20160829 20160728 20160831 EXP US-JNJFOC-20160719684 JANSSEN 70.67 YR E M Y 0.00000 20160831 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
126019832 12601983 1 SS STELARA USTEKINUMAB 1 Subcutaneous N N 14E021ML 0 45 MG SOLUTION FOR INJECTION
126019832 12601983 2 SS STELARA USTEKINUMAB 1 Subcutaneous N N 14E021ML 0 45 MG SOLUTION FOR INJECTION
126019832 12601983 3 SS STELARA USTEKINUMAB 1 Subcutaneous N N 14E021ML 0 45 MG SOLUTION FOR INJECTION
126019832 12601983 4 PS STELARA USTEKINUMAB 1 Subcutaneous N N 14E021ML 125261 45 MG SOLUTION FOR INJECTION
126019832 12601983 5 SS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126019832 12601983 1 Psoriatic arthropathy
126019832 12601983 2 Psoriatic arthropathy
126019832 12601983 3 Psoriasis
126019832 12601983 4 Psoriasis
126019832 12601983 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126019832 12601983 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126019832 12601983 Dizziness
126019832 12601983 Lung neoplasm malignant

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
126019832 12601983 1 20160422 2016 0
126019832 12601983 2 20150515 0
126019832 12601983 3 20150515 0
126019832 12601983 4 20160422 2016 0