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
126118291 12611829 1 I 20110801 20151026 20160801 20160801 PER US-PFIZER INC-3061086 PFIZER 57.00 YR F Y 0.00000 20160801 MD 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
126118291 12611829 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 15 MG, WEEKLY UNK 11719 15 MG
126118291 12611829 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 10 MG, WEEKLY UNK 11719 10 MG
126118291 12611829 3 SS FOLIC ACID. FOLIC ACID 1 1 MG, FREQ: 1 DAY, INTERVAL: 1 UNK 0 1 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126118291 12611829 1 Synovitis
126118291 12611829 3 Synovitis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126118291 12611829 Elbow deformity
126118291 12611829 Fatigue
126118291 12611829 Foot deformity
126118291 12611829 Hand deformity
126118291 12611829 Joint swelling
126118291 12611829 Musculoskeletal stiffness
126118291 12611829 Pain
126118291 12611829 Therapy non-responder

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
126118291 12611829 1 20110801 0
126118291 12611829 2 20110301 0
126118291 12611829 3 20110301 0