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
125854701 12585470 1 I 20160712 20160724 20160724 PER US-AMGEN-USASP2016090874 AMGEN 54.00 YR A M Y 0.00000 20160724 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
125854701 12585470 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
125854701 12585470 2 SS HUMIRA ADALIMUMAB 1 Unknown UNK 0
125854701 12585470 3 SS STELARA USTEKINUMAB 1 Unknown UNK 0
125854701 12585470 4 SS OTEZLA APREMILAST 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125854701 12585470 1 Psoriasis
125854701 12585470 2 Psoriasis
125854701 12585470 3 Psoriasis
125854701 12585470 4 Psoriasis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125854701 12585470 Drug ineffective
125854701 12585470 Dyspnoea
125854701 12585470 Feeding disorder
125854701 12585470 Nausea
125854701 12585470 Rash
125854701 12585470 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found