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
127026091 12702609 1 I 201606 20160619 20160831 20160831 PER US-JNJFOC-20160617744 JANSSEN 52.51 YR A M Y 69.85000 KG 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
127026091 12702609 1 PS STELARA USTEKINUMAB 1 Subcutaneous N UNKNOWN 125261 45 MG SOLUTION FOR INJECTION
127026091 12702609 2 C TRAMADOL. TRAMADOL 1 Unknown 0 50 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127026091 12702609 1 Psoriasis
127026091 12702609 2 Myalgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127026091 12702609 Dysphagia
127026091 12702609 Impaired work ability
127026091 12702609 Insomnia
127026091 12702609 Nausea
127026091 12702609 Oropharyngeal pain
127026091 12702609 Pruritus
127026091 12702609 Psoriasis
127026091 12702609 Retching
127026091 12702609 Vision blurred

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
127026091 12702609 1 20160617 0
127026091 12702609 2 201606 0