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
126119511 12611951 1 I 20160315 20160801 20160801 PER US-PFIZER INC-3219465 PFIZER 35.00 YR M 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
126119511 12611951 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 INJECTION UNK 11719 SOLUTION FOR INJECTION
126119511 12611951 2 SS ENBREL ETANERCEPT 1 UNK UNK 0
126119511 12611951 3 SS HUMIRA ADALIMUMAB 1 UNK UNK 0
126119511 12611951 4 SS SULFASALAZINE. SULFASALAZINE 1 UNK UNK 0
126119511 12611951 5 C XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, FREQ: 2 DAY; INTERVAL:1 UNK 0 5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126119511 12611951 1 Rheumatoid arthritis
126119511 12611951 2 Rheumatoid arthritis
126119511 12611951 3 Rheumatoid arthritis
126119511 12611951 4 Rheumatoid arthritis
126119511 12611951 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126119511 12611951 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126119511 12611951 Drug ineffective
126119511 12611951 Nausea

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
126119511 12611951 1 20140101 0
126119511 12611951 2 20130101 20140101 0
126119511 12611951 3 20130101 20140101 0
126119511 12611951 4 20130101 20140101 0