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
126261571 12626157 1 I 20160720 20160805 20160805 EXP 00501148 CA-HQ SPECIALTY-CA-2016INT000673 INTERCHEM 75.00 YR F Y 0.00000 20160805 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
126261571 12626157 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK U 201749
126261571 12626157 2 SS ENBREL ETANERCEPT 1 Unknown UNK U 0
126261571 12626157 3 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK U 0
126261571 12626157 4 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK U 0
126261571 12626157 5 SS PREDNISONE. PREDNISONE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126261571 12626157 1 Rheumatoid arthritis
126261571 12626157 2 Rheumatoid arthritis
126261571 12626157 3 Rheumatoid arthritis
126261571 12626157 4 Rheumatoid arthritis
126261571 12626157 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126261571 12626157 HO
126261571 12626157 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126261571 12626157 Condition aggravated
126261571 12626157 Vertigo

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

no results found

Therapies reported

no results found