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
125487502 12548750 2 F 20160702 20160711 20160712 20160715 EXP CN-SA-2016SA126878 AVENTIS 30.00 YR A F Y 44.00000 KG 20160715 CN CN CN

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
125487502 12548750 1 PS THYMOGLOBULINE LAPINE T-LYMPHOCYTE IMMUNE GLOBULIN 1 Unknown 9.88MG/KG TOTALLY 17 VIALS U C4180C02 103869 9.88 MG/KG
125487502 12548750 2 C BUSULFEX BUSULFAN 1 0
125487502 12548750 3 C CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125487502 12548750 1 Aplastic anaemia

Outcome of event

Event ID CASEID OUTC COD
125487502 12548750 DE
125487502 12548750 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125487502 12548750 Cardiac failure
125487502 12548750 Dyspnoea
125487502 12548750 Engraftment syndrome
125487502 12548750 Lung infection
125487502 12548750 Pulmonary alveolar haemorrhage
125487502 12548750 Pyrexia
125487502 12548750 Respiratory failure

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
125487502 12548750 1 20160614 0
125487502 12548750 2 20160614 0
125487502 12548750 3 20160614 0