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
126562962 12656296 2 F 20160812 20160812 20160816 20160819 EXP BR-BIOMARINAP-BR-2016-110729 BIOMARIN 9.52 YR M Y 0.00000 20160819 CN BR BR

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
126562962 12656296 1 PS VIMIZIM ELOSULFASE ALFA 1 Intravenous (not otherwise specified) UNK NOT REPORTED 125460 SOLUTION FOR INFUSION
126562962 12656296 2 C CLEXANE ENOXAPARIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126562962 12656296 1 Mucopolysaccharidosis IV
126562962 12656296 2 Thrombosis

Outcome of event

Event ID CASEID OUTC COD
126562962 12656296 HO
126562962 12656296 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126562962 12656296 Coma
126562962 12656296 Death
126562962 12656296 Haemorrhage
126562962 12656296 Nosocomial infection
126562962 12656296 Thrombosis

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
126562962 12656296 1 20141016 0