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
123851214 12385121 4 F 2016 20160627 20160519 20160706 EXP LB-SA-2016SA095144 AVENTIS 24.00 YR A F Y 51.00000 KG 20160706 CN LB LB

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
123851214 12385121 1 PS CEREZYME IMIGLUCERASE 1 Intravenous (not otherwise specified) DOSE: 7 VIALS OF 400 U (HALF DOSE) U UNKNOWN 20367 POWDER FOR SOLUTION FOR INFUSION QOW
123851214 12385121 2 SS CEREZYME IMIGLUCERASE 1 Intravenous (not otherwise specified) DOSE: 7 VIALS OF 400 U (HALF DOSE) U UNKNOWN 20367 POWDER FOR SOLUTION FOR INFUSION QOW
123851214 12385121 3 C ALDACTONE SPIRONOLACTONE 1 Oral 0 25 MG BID
123851214 12385121 4 C LASIX FUROSEMIDE 1 Oral 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123851214 12385121 1 Gaucher's disease type I
123851214 12385121 2 Gaucher's disease type I
123851214 12385121 3 Diuretic therapy
123851214 12385121 4 Diuretic therapy

Outcome of event

Event ID CASEID OUTC COD
123851214 12385121 DS
123851214 12385121 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123851214 12385121 Blindness
123851214 12385121 Disease progression
123851214 12385121 Hypoacusis
123851214 12385121 Hypokinesia
123851214 12385121 Loss of consciousness
123851214 12385121 Seizure
123851214 12385121 Tremor
123851214 12385121 Underdose
123851214 12385121 Visual impairment
123851214 12385121 Weight decreased

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

no results found

Therapies reported

no results found