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
126721933 12672193 3 F 20160801 20160913 20160822 20160919 EXP JP-PFIZER INC-2016394308 PFIZER 86.00 YR F Y 0.00000 20160919 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
126721933 12672193 1 PS RHEUMATREX METHOTREXATE SODIUM 1 Oral 4 MG, WEEKLY 11719 4 MG CAPSULE /wk
126721933 12672193 2 SS RHEUMATREX METHOTREXATE SODIUM 1 Oral 6 MG, WEEKLY 11719 6 MG CAPSULE /wk
126721933 12672193 3 SS RHEUMATREX METHOTREXATE SODIUM 1 Oral 8 MG, WEEKLY 11719 8 MG CAPSULE /wk
126721933 12672193 4 C MIZORIBINE MIZORIBINE 1 Oral 75 MG, DAILY 0 75 MG TABLET
126721933 12672193 5 C AZULFIDINE EN-TABS SULFASALAZINE 1 Oral 1000 MG, DAILY 0 1000 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126721933 12672193 1 Rheumatoid arthritis
126721933 12672193 4 Rheumatoid arthritis
126721933 12672193 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126721933 12672193 HO
126721933 12672193 LT
126721933 12672193 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126721933 12672193 Colon cancer
126721933 12672193 Therapeutic response decreased

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
126721933 12672193 1 20100303 20150817 0
126721933 12672193 2 20150818 20151012 0
126721933 12672193 3 20151013 0
126721933 12672193 4 20140819 0