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
125320691 12532069 1 I 20160628 20160706 20160706 EXP IT-FRESENIUS KABI-FK201604098 FRESENIUS KABI 44.00 YR F Y 0.00000 20160706 OT IT IT

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
125320691 12532069 1 PS CYTARABINE (Manufacturer Unknown) CYTARABINE 1 Unknown U UNKNOWN 76512 UNKNOWN
125320691 12532069 2 SS FLUDARABINE PHOSPHATE. FLUDARABINE PHOSPHATE 1 0
125320691 12532069 3 SS IDARUBICIN IDARUBICIN 1 0
125320691 12532069 4 C POSACONAZOLE POSACONAZOLE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125320691 12532069 1 Acute promyelocytic leukaemia
125320691 12532069 2 Acute promyelocytic leukaemia
125320691 12532069 3 Acute promyelocytic leukaemia
125320691 12532069 4 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125320691 12532069 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125320691 12532069 Bronchopulmonary aspergillosis
125320691 12532069 Pyrexia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found