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
126183681 12618368 1 I 2015 20160315 20160803 20160803 PER US-PFIZER INC-2016162141 PFIZER 47.00 YR M Y 0.00000 20160803 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
126183681 12618368 1 SS ENBREL ETANERCEPT 1 50 MG, UNK 0 50 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
126183681 12618368 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 2.5 MG, FREQ: 6 WEEK; INTERVAL: 1 11719 2.5 MG
126183681 12618368 3 SS NAPROXEN. NAPROXEN 1 UNK 0
126183681 12618368 4 SS HUMIRA ADALIMUMAB 1 40 MG, UNK 0 40 MG
126183681 12618368 5 C XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 0 5 MG TABLET BID
126183681 12618368 6 C XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, UNK (FREQ: 2 DAY; INTERVAL: 1) 0 5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126183681 12618368 1 Rheumatoid arthritis
126183681 12618368 2 Rheumatoid arthritis
126183681 12618368 3 Rheumatoid arthritis
126183681 12618368 4 Rheumatoid arthritis
126183681 12618368 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126183681 12618368 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126183681 12618368 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
126183681 12618368 1 20160101 0
126183681 12618368 2 20160101 0
126183681 12618368 3 20160301 0
126183681 12618368 4 20150701 20150801 0