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
126092462 12609246 2 F 20160720 20160727 20160801 20160804 PER CA-AMGEN-CANSP2016097119 AMGEN 79.00 YR E F Y 0.00000 20160804 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
126092462 12609246 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, QWK 103795 50 MG UNKNOWN FORMULATION /wk
126092462 12609246 2 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown 400 MG, QD 0 400 MG QD
126092462 12609246 3 SS METHOTREXATE. METHOTREXATE 1 Unknown 20 MG, QWK 0 20 MG /wk
126092462 12609246 4 C TYLENOL ACETAMINOPHEN 1 UNK 0
126092462 12609246 5 C IRON IRON 1 UNK, AT NIGHT 0
126092462 12609246 6 C METOPROLOL. METOPROLOL 1 UNK, AT NIGHT 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126092462 12609246 1 Rheumatoid arthritis
126092462 12609246 2 Rheumatoid arthritis
126092462 12609246 3 Rheumatoid arthritis
126092462 12609246 4 Rheumatoid arthritis
126092462 12609246 5 Rheumatoid arthritis
126092462 12609246 6 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126092462 12609246 Arthralgia
126092462 12609246 Arthritis
126092462 12609246 Drug ineffective
126092462 12609246 Gait disturbance
126092462 12609246 Joint swelling
126092462 12609246 Pain in extremity
126092462 12609246 Rash

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126092462 12609246 1 201409 201605 0
126092462 12609246 2 201402 0
126092462 12609246 3 201311 201501 0