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
115178163 11517816 3 F 2015 20160810 20150917 20160818 EXP CA-PFIZER INC-2015272087 PFIZER 75.00 YR F Y 0.00000 20160818 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
115178163 11517816 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 25 MG, WEEKLY N 11719 25 MG /wk
115178163 11517816 2 SS SULFASALAZINE. SULFASALAZINE 1 UNK U 7073
115178163 11517816 3 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK U 0
115178163 11517816 4 SS LEFLUNOMIDE. LEFLUNOMIDE 1 20 MG, DAILY N 0 20 MG
115178163 11517816 5 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115178163 11517816 1 Rheumatoid arthritis
115178163 11517816 2 Rheumatoid arthritis
115178163 11517816 3 Rheumatoid arthritis
115178163 11517816 4 Rheumatoid arthritis
115178163 11517816 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
115178163 11517816 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
115178163 11517816 Abdominal discomfort
115178163 11517816 Arthropathy
115178163 11517816 Death
115178163 11517816 Drug intolerance
115178163 11517816 Localised infection
115178163 11517816 Nausea
115178163 11517816 Pain
115178163 11517816 Purulent discharge
115178163 11517816 Treatment failure
115178163 11517816 Vomiting

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
115178163 11517816 1 20141006 20150330 0
115178163 11517816 4 20150303 20150708 0