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
125005532 12500553 2 F 2016 20160711 20160627 20160725 EXP GB-JNJFOC-20160622052 JANSSEN 67.09 YR E M Y 0.00000 20160725 CN 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
125005532 12500553 1 SS STELARA USTEKINUMAB 1 Subcutaneous Y U UNKNOWN 0 45 MG SOLUTION FOR INJECTION
125005532 12500553 2 PS STELARA USTEKINUMAB 1 Subcutaneous Y U UNKNOWN 125261 45 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125005532 12500553 1 Psoriasis
125005532 12500553 2 Psoriasis

Outcome of event

Event ID CASEID OUTC COD
125005532 12500553 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125005532 12500553 Depression
125005532 12500553 Dyspnoea
125005532 12500553 Lower respiratory tract infection
125005532 12500553 Nasal obstruction
125005532 12500553 Oropharyngeal pain
125005532 12500553 Oxygen saturation decreased
125005532 12500553 Psoriasis
125005532 12500553 Rhinorrhoea
125005532 12500553 Sinus 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
125005532 12500553 1 20150814 0