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
125834111 12583411 1 I 20160714 20160722 20160722 EXP CA-PFIZER INC-2016353416 PFIZER 40.00 YR M Y 0.00000 20160722 CN CA CA

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
125834111 12583411 1 SS ENBREL ETANERCEPT 1 UNK U 0
125834111 12583411 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK U 11719
125834111 12583411 3 SS HUMIRA ADALIMUMAB 1 Unknown UNK U 0
125834111 12583411 4 SS NEORAL CYCLOSPORINE 1 Oral UNK U 0
125834111 12583411 5 SS REMICADE INFLIXIMAB 1 Unknown UNK U 0
125834111 12583411 6 SS SECUKINUMAB SECUKINUMAB 1 Subcutaneous 300 MG, QWK U 0 300 MG INJECTION /wk
125834111 12583411 7 SS SORIATANE ACITRETIN 1 Unknown UNK U 0 CAPSULE
125834111 12583411 8 SS STELARA USTEKINUMAB 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125834111 12583411 4 Psoriasis
125834111 12583411 6 Psoriasis

Outcome of event

Event ID CASEID OUTC COD
125834111 12583411 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125834111 12583411 Drug ineffective
125834111 12583411 Headache
125834111 12583411 Injection site haemorrhage
125834111 12583411 Injection site swelling
125834111 12583411 Insomnia
125834111 12583411 Muscular weakness
125834111 12583411 Myalgia
125834111 12583411 Nausea
125834111 12583411 Pain in extremity
125834111 12583411 Psoriasis
125834111 12583411 Vein rupture

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

no results found

Therapies reported

no results found