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
126897211 12689721 1 I 20160817 20160826 20160826 EXP CA-PFIZER INC-2016400948 PFIZER 0.00 F Y 0.00000 20160826 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
126897211 12689721 1 SS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, UNK U 0 50 MG
126897211 12689721 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous 20 MG, UNK U 11719 20 MG SOLUTION FOR INJECTION
126897211 12689721 3 SS NEORAL CYCLOSPORINE 1 Oral 20 MG, UNK U 0 20 MG
126897211 12689721 4 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 20 MG, UNK U 0 20 MG
126897211 12689721 5 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) 3 MG/KG, UNK U 0 3 MG/KG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126897211 12689721 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126897211 12689721 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126897211 12689721 C-reactive protein abnormal
126897211 12689721 Drug ineffective

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

no results found

Therapies reported

no results found