The Safety Rates Drug Report

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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
125213831 12521383 1 I 20150701 20150928 20160701 20160701 PER US-PFIZER INC-3028191 PFIZER 0.00 F Y 0.00000 20160701 OT 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
125213831 12521383 1 PS ARTHROTEC DICLOFENAC SODIUMMISOPROSTOL 1 U UNK 20607 TABLET
125213831 12521383 2 SS CELEBREX CELECOXIB 1 U UNK 20998 CAPSULE, HARD
125213831 12521383 3 SS ENBREL ETANERCEPT 1 U UNK 0
125213831 12521383 4 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 U UNK 11719
125213831 12521383 5 SS CIMZIA CERTOLIZUMAB PEGOL 1 U UNK 0
125213831 12521383 6 SS HUMIRA ADALIMUMAB 1 U UNK 0
125213831 12521383 7 SS OTEZLA APREMILAST 1 U UNK 0
125213831 12521383 8 SS REMICADE INFLIXIMAB 1 U UNK 0
125213831 12521383 9 SS SIMPONI GOLIMUMAB 1 U UNK 0
125213831 12521383 10 SS PREDNISONE. PREDNISONE 1 U UNK 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125213831 12521383 Musculoskeletal deformity
125213831 12521383 Pain

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

no results found

Therapies reported

no results found