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
123238732 12323873 2 F 20160725 20160502 20160728 EXP CA-AMGEN-CANSP2016054148 AMGEN 45.00 YR A F Y 76.00000 KG 20160728 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
123238732 12323873 1 PS ENBREL ETANERCEPT 1 Unknown UNK UNK, QWK U 103795 UNKNOWN FORMULATION /wk
123238732 12323873 2 SS HUMIRA ADALIMUMAB 1 Unknown UNK 0
123238732 12323873 3 SS IBUPROFEN. IBUPROFEN 1 Unknown UNK 0
123238732 12323873 4 SS ORENCIA ABATACEPT 1 Unknown UNK 0
123238732 12323873 5 SS REMICADE INFLIXIMAB 1 Unknown UNK 0
123238732 12323873 6 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) UNK 0
123238732 12323873 7 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Oral 200 MG, BID 0 200 MG BID
123238732 12323873 8 C METHOTREXATE. METHOTREXATE 1 Oral 10 MG, QWK 0 10 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123238732 12323873 1 Rheumatoid arthritis
123238732 12323873 2 Rheumatoid arthritis
123238732 12323873 3 Rheumatoid arthritis
123238732 12323873 4 Rheumatoid arthritis
123238732 12323873 5 Rheumatoid arthritis
123238732 12323873 6 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
123238732 12323873 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123238732 12323873 Drug ineffective
123238732 12323873 Injection site reaction
123238732 12323873 Renal impairment
123238732 12323873 Rheumatoid arthritis
123238732 12323873 Throat tightness

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

no results found

Therapies reported

no results found