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
125389361 12538936 1 I 20160612 0 20160707 20160707 DIR 15.12 YR F N 87.50000 KG 20160612 N 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
125389361 12538936 1 PS CYTARABINE. CYTARABINE 1 0 15270 MG
125389361 12538936 3 C MITOXANTRONE HYDROCHLORIDE. MITOXANTRONE HYDROCHLORIDE 1 0 92 MG
125389361 12538936 4 SS DAUNORUBICIN DAUNORUBICIN 1 0
125389361 12538936 6 SS ETOPOSIDE (VP-16) ETOPOSIDE 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125389361 12538936 HO
125389361 12538936 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125389361 12538936 Erythema
125389361 12538936 Genital lesion
125389361 12538936 Gram stain positive
125389361 12538936 Hypotension
125389361 12538936 Necrotising fasciitis
125389361 12538936 Oedema
125389361 12538936 Pain
125389361 12538936 Pseudomonas test positive
125389361 12538936 Sepsis
125389361 12538936 Tachypnoea

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
125389361 12538936 1 20160531 0
125389361 12538936 3 20160602 0
125389361 12538936 4 20160125 0
125389361 12538936 6 20160312 0