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
105529862 10552986 2 F 20160812 20141029 20160818 PER US-PFIZER INC-2014297300 PFIZER 61.00 YR F Y 0.00000 20160818 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
105529862 10552986 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY U 203214 5 MG TABLET BID
105529862 10552986 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK 11719
105529862 10552986 3 SS HUMIRA ADALIMUMAB 1 UNK 0
105529862 10552986 4 SS ARAVA LEFLUNOMIDE 1 UNK 0
105529862 10552986 5 SS ORENCIA ABATACEPT 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105529862 10552986 1 Rheumatoid arthritis
105529862 10552986 2 Rheumatoid arthritis
105529862 10552986 3 Rheumatoid arthritis
105529862 10552986 4 Rheumatoid arthritis
105529862 10552986 5 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
105529862 10552986 Drug ineffective

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
105529862 10552986 2 2011 201303 0
105529862 10552986 4 201303 201409 0
105529862 10552986 5 201309 201406 0