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
126518441 12651844 1 I 2015 20160330 20160815 20160815 EXP US-JNJFOC-20160329091 JANSSEN 0.00 E F Y 0.00000 20160815 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
126518441 12651844 1 SS STELARA USTEKINUMAB 1 Subcutaneous N UNKNOWN 0 SOLUTION FOR INJECTION
126518441 12651844 2 PS STELARA USTEKINUMAB 1 Subcutaneous N UNKNOWN 125261 SOLUTION FOR INJECTION
126518441 12651844 3 C OTEZLA APREMILAST 1 Unknown 0 UNSPECIFIED
126518441 12651844 4 C OTEZLA APREMILAST 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126518441 12651844 1 Psoriasis
126518441 12651844 2 Psoriatic arthropathy
126518441 12651844 3 Psoriasis
126518441 12651844 4 Psoriatic arthropathy

Outcome of event

Event ID CASEID OUTC COD
126518441 12651844 OT
126518441 12651844 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126518441 12651844 Anaemia
126518441 12651844 Blood glucose decreased
126518441 12651844 Dehydration
126518441 12651844 Drug ineffective
126518441 12651844 Dysstasia
126518441 12651844 Fall
126518441 12651844 Fatigue
126518441 12651844 Hospitalisation
126518441 12651844 Malaise
126518441 12651844 Peripheral swelling
126518441 12651844 Syncope

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
126518441 12651844 1 2015 0
126518441 12651844 2 2015 0
126518441 12651844 3 2015 0
126518441 12651844 4 2015 0