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
124168582 12416858 2 F 20151113 20160831 20160530 20160906 EXP JP-PFIZER INC-2015393908 PFIZER 80.00 YR F Y 54.00000 KG 20160906 MD JP JP

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
124168582 12416858 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 2120 MG Y 203214 5 MG TABLET BID
124168582 12416858 2 SS RHEUMATREX METHOTREXATE SODIUM 1 Oral 6 MG, WEEKLY 2262 MG Y 11719 6 MG CAPSULE /wk
124168582 12416858 3 C BLOPRESS CANDESARTAN CILEXETIL 1 Oral 0
124168582 12416858 4 C AMLODIN AMLODIPINE BESYLATE 1 Oral 0
124168582 12416858 5 C SELBEX TEPRENONE 1 Oral 0
124168582 12416858 6 C TAKEPRON LANSOPRAZOLE 1 Oral 0
124168582 12416858 7 C FLOMOX CEFCAPENE PIVOXIL HYDROCHLORIDE HYDRATE 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124168582 12416858 1 Rheumatoid arthritis
124168582 12416858 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
124168582 12416858 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124168582 12416858 Interstitial lung disease

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
124168582 12416858 1 20150413 20151110 0
124168582 12416858 2 20080826 20151110 0
124168582 12416858 7 20151110 0