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
122222974 12222297 4 F 20160320 20160811 20160330 20160818 EXP CA-JNJFOC-20160321537 PHARMACYCLICS 73.69 YR E M Y 0.00000 20160818 OT CA CA

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
122222974 12222297 1 PS IMBRUVICA IBRUTINIB 1 Oral Y N 205552 560 MG CAPSULE QD
122222974 12222297 2 SS FRAGMIN DALTEPARIN SODIUM 1 Unknown U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122222974 12222297 1 Mantle cell lymphoma
122222974 12222297 2 Pulmonary embolism

Outcome of event

Event ID CASEID OUTC COD
122222974 12222297 OT
122222974 12222297 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122222974 12222297 Contusion
122222974 12222297 Diarrhoea
122222974 12222297 Fatigue
122222974 12222297 Haematochezia
122222974 12222297 Haemoglobin decreased
122222974 12222297 Intervertebral disc degeneration
122222974 12222297 Nausea
122222974 12222297 Rash

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
122222974 12222297 1 20160310 20160418 0