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
124261743 12426174 3 F 20160515 20160829 20160601 20160901 PER US-PFIZER INC-2016284058 PFIZER 67.00 YR F Y 0.00000 20160901 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
124261743 12426174 1 PS XELJANZ XR TOFACITINIB CITRATE 1 11 MG, 1X/DAY U N30256 208246 11 MG PROLONGED-RELEASE TABLET QD
124261743 12426174 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 2.5 MG, UNK U 11719 2.5 MG
124261743 12426174 3 SS FOLIC ACID. FOLIC ACID 1 1 MG, UNK U 5897 1 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124261743 12426174 1 Rheumatoid arthritis
124261743 12426174 2 Rheumatoid arthritis
124261743 12426174 3 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124261743 12426174 Nasopharyngitis
124261743 12426174 Paranasal sinus discomfort
124261743 12426174 Sinus headache

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
124261743 12426174 1 20160515 0