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
126118571 12611857 1 I 20160223 20160801 20160801 PER US-PFIZER INC-3194265 PFIZER 64.00 YR F Y 0.00000 20160801 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
126118571 12611857 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK UNK 11719
126118571 12611857 2 SS AZULFIDINE SULFASALAZINE 1 UNK U UNK 0
126118571 12611857 3 SS CIMZIA CERTOLIZUMAB PEGOL 1 UNK U UNK 0
126118571 12611857 4 SS ENBREL ETANERCEPT 1 UNK U UNK 0
126118571 12611857 5 SS PLAQUENIL/00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 UNK U UNK 0
126118571 12611857 6 SS GOLD GOLD 1 UNK U UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126118571 12611857 1 Rheumatoid arthritis
126118571 12611857 2 Rheumatoid arthritis
126118571 12611857 3 Rheumatoid arthritis
126118571 12611857 4 Rheumatoid arthritis
126118571 12611857 5 Rheumatoid arthritis
126118571 12611857 6 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126118571 12611857 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126118571 12611857 Drug ineffective
126118571 12611857 Drug intolerance

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
126118571 12611857 1 20020923 0