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
125529174 12552917 4 F 201606 20160908 20160713 20160914 EXP CA-JNJFOC-20160706916 PHARMACYCLICS 80.38 YR E F Y 0.00000 20160914 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
125529174 12552917 1 SS IMBRUVICA IBRUTINIB 1 Oral Y N 0 420 MG CAPSULE QD
125529174 12552917 2 SS IMBRUVICA IBRUTINIB 1 Oral Y N 0 280 MG CAPSULE QD
125529174 12552917 3 PS IMBRUVICA IBRUTINIB 1 Oral Y N 205552 280 MG CAPSULE QD
125529174 12552917 4 SS AMOXICILLIN. AMOXICILLIN 1 Oral Y 0 3 DF UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125529174 12552917 1 Chronic lymphocytic leukaemia
125529174 12552917 2 Chronic lymphocytic leukaemia
125529174 12552917 3 Chronic lymphocytic leukaemia
125529174 12552917 4 Pyrexia

Outcome of event

Event ID CASEID OUTC COD
125529174 12552917 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125529174 12552917 Angina pectoris
125529174 12552917 Cough
125529174 12552917 Haemoglobin decreased
125529174 12552917 Malaise
125529174 12552917 Nasopharyngitis
125529174 12552917 Neutrophil count decreased
125529174 12552917 Pruritus
125529174 12552917 Pyrexia
125529174 12552917 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
125529174 12552917 1 20160603 20160609 0
125529174 12552917 2 20160616 20160623 0
125529174 12552917 3 20160629 0
125529174 12552917 4 20160718 20160719 0