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
127790131 12779013 1 I 20160908 0 20160921 20160921 DIR FDA-CTU 69.44 YR M N 86.40000 KG 20160920 N 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
127790131 12779013 2 PS METHOTREXATE. METHOTREXATE 1 0 17.3 G
127790131 12779013 3 SS LEUCOVORIN CALCIUM. LEUCOVORIN CALCIUM 1 0 2808 MG
127790131 12779013 4 SS RITUXIMAB (MOAB C2B8 ANTI CD20, CHIMERIC) RITUXIMAB 1 0 800 MG
127790131 12779013 5 SS TEMOZOLOMIDE. TEMOZOLOMIDE 1 0 1625 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127790131 12779013 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127790131 12779013 Chondrocalcinosis pyrophosphate
127790131 12779013 Disease progression
127790131 12779013 Hyponatraemia
127790131 12779013 Mental status changes
127790131 12779013 Muscular weakness
127790131 12779013 Neutropenia
127790131 12779013 Pain in extremity
127790131 12779013 Pyrexia

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
127790131 12779013 2 20160818 0
127790131 12779013 3 20160822 0
127790131 12779013 4 20160819 0
127790131 12779013 5 20160828 0