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
107546346 10754634 6 F 20160624 20160624 20150202 20160701 EXP BR-SA-2015SA010881 AVENTIS 41.00 YR A F Y 64.00000 KG 20160701 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
107546346 10754634 1 PS CEREZYME IMIGLUCERASE 1 Intravenous (not otherwise specified) 2 VIALS C3150C04 20367 POWDER FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107546346 10754634 1 Gaucher's disease

Outcome of event

Event ID CASEID OUTC COD
107546346 10754634 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
107546346 10754634 Arthropathy
107546346 10754634 Bone disorder
107546346 10754634 Gait disturbance
107546346 10754634 Limb asymmetry
107546346 10754634 Oedema peripheral

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
107546346 10754634 1 20140301 0