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
115881373 11588137 3 F 20160712 20151002 20160718 EXP CA-AMGEN-CANSP2015101752 AMGEN 70.00 YR E M Y 0.00000 20160717 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
115881373 11588137 1 PS ENBREL ETANERCEPT 1 Subcutaneous UNK U 103795 UNKNOWN FORMULATION
115881373 11588137 2 SS SULFASALAZINE. SULFASALAZINE 1 Unknown UNK 0
115881373 11588137 3 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK 0
115881373 11588137 4 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0 TABLET
115881373 11588137 5 SS GOLD GOLD 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115881373 11588137 1 Rheumatoid arthritis
115881373 11588137 2 Rheumatoid arthritis
115881373 11588137 3 Rheumatoid arthritis
115881373 11588137 4 Rheumatoid arthritis
115881373 11588137 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
115881373 11588137 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115881373 11588137 Acute kidney injury
115881373 11588137 Drug effect decreased
115881373 11588137 Pain

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

no results found

Therapies reported

no results found