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
125576171 12557617 1 I 20131014 20130910 20160714 20160714 EXP HU-JNJFOC-20131006295 JANSSEN 6.00 DEC A M Y 0.00000 20160712 CN HU HU

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
125576171 12557617 1 PS STELARA USTEKINUMAB 1 Subcutaneous N 125261 90 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125576171 12557617 1 Psoriasis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125576171 12557617 Body temperature decreased
125576171 12557617 Fatigue
125576171 12557617 Hepatic function abnormal
125576171 12557617 Nasopharyngitis
125576171 12557617 Oropharyngeal pain
125576171 12557617 Productive cough
125576171 12557617 Thyroid cyst
125576171 12557617 Vomiting

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
125576171 12557617 1 20130902 0