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
125644111 12564411 1 I 20160712 20160718 20160718 EXP CA-AMGEN-CANSP2016091143 AMGEN 75.00 YR E F Y 0.00000 20160717 OT 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
125644111 12564411 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
125644111 12564411 2 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0
125644111 12564411 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK 0
125644111 12564411 4 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
125644111 12564411 5 SS PREDNISONE. PREDNISONE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125644111 12564411 1 Rheumatoid arthritis
125644111 12564411 2 Rheumatoid arthritis
125644111 12564411 3 Rheumatoid arthritis
125644111 12564411 4 Rheumatoid arthritis
125644111 12564411 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125644111 12564411 HO
125644111 12564411 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125644111 12564411 Condition aggravated
125644111 12564411 Mobility decreased
125644111 12564411 Rheumatoid arthritis
125644111 12564411 Vertigo

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

no results found

Therapies reported

no results found