The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6919963 7494515 F 6919963-5 20100423 20100712 20100811 EXP FR-GENZYME-CLOF-1000938 GENZYMEP 60 YR M Y 95 KG 20100811 OT FRANCE

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6919963 1014396127 PS EVOLTRA 2 INTRAVENOUS 60 MG/M2, QD UNKNOWN 21673
6919963 1014396128 C POLARAMINE 1 UNK
6919963 1014396129 C ZOPHREN 2 1 OTHER, UNK
6919963 1014396130 C ZYLORIC 2 300 MG, UNK
6919963 1014396131 C NOXAFIL 1 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6919963 1014396127 ACUTE LYMPHOCYTIC LEUKAEMIA
6919963 1014396128 PROPHYLAXIS
6919963 1014396129 PROPHYLAXIS
6919963 1014396130 PROPHYLAXIS
6919963 1014396131 ANTIFUNGAL TREATMENT

Outcome of event

Event ID OUTC COD
6919963 LT
6919963 OT

Reactions reported

Event ID PT
6919963 CYTOLYTIC HEPATITIS
6919963 HEPATITIS B CORE ANTIGEN POSITIVE
6919963 HEPATITIS B SURFACE ANTIGEN POSITIVE

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6919963 1014396127 20100421 20100423 3 DAY
6919963 1014396128 20100421 20100521 31 DAY
6919963 1014396129 20100421 20100524 34 DAY
6919963 1014396130 20100422 20100508 17 DAY
6919963 1014396131 20100420 20100521 32 DAY