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
125721691 12572169 1 I 20160712 20160719 20160719 EXP CA-PFIZER INC-2016348773 PFIZER 75.00 YR F Y 0.00000 20160719 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
125721691 12572169 1 SS ENBREL ETANERCEPT 1 Unknown UNK U 0
125721691 12572169 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK U 11719
125721691 12572169 3 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK U 0
125721691 12572169 4 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK U 0
125721691 12572169 5 SS PREDNISONE. PREDNISONE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125721691 12572169 1 Rheumatoid arthritis
125721691 12572169 2 Rheumatoid arthritis
125721691 12572169 3 Rheumatoid arthritis
125721691 12572169 4 Rheumatoid arthritis
125721691 12572169 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125721691 12572169 OT
125721691 12572169 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125721691 12572169 Condition aggravated
125721691 12572169 Mobility decreased
125721691 12572169 Rheumatoid arthritis
125721691 12572169 Vertigo

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

no results found

Therapies reported

no results found