The Safety Rates Drug Report

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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
125905301 12590530 1 I 20160715 20160725 20160725 PER US-AMGEN-USASP2016093601 AMGEN 0.00 A F Y 0.00000 20160725 CN US US

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
125905301 12590530 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
125905301 12590530 2 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
125905301 12590530 3 SS ARAVA LEFLUNOMIDE 1 Unknown UNK 0
125905301 12590530 4 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0
125905301 12590530 5 SS SULFASALAZINE. SULFASALAZINE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125905301 12590530 1 Rheumatoid arthritis
125905301 12590530 2 Rheumatoid arthritis
125905301 12590530 3 Rheumatoid arthritis
125905301 12590530 4 Rheumatoid arthritis
125905301 12590530 5 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125905301 12590530 Adverse drug reaction
125905301 12590530 Infection
125905301 12590530 Treatment failure

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

no results found

Therapies reported

no results found