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
6549565 7071213 F 3 6549565-4 20090703 20100105 20100119 EXP MOZO-1000230 GENZYME YR M N 65 KG 20100115 MD NETHERLANDS

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
6549565 1012992247 PS PLERIXAFOR (PLERIXAFOR) SOLUTION FOR INJECTION 2 SUBCUTANEOUS 0.78 ML, SUBCUTANEOUS U U 09-000446 20090901 22311
6549565 1013024715 C ACETAMINOPHEN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6549565 1012992247 HAEMATOPOIETIC STEM CELL MOBILISATION

Outcome of event

Event ID OUTC COD
6549565 HO

Reactions reported

Event ID PT
6549565 DIARRHOEA
6549565 DYSPNOEA
6549565 TACHYCARDIA

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

Event ID RPSR COD
6549565 FGN
6549565 HP
6549565 OTH
6549565 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6549565 1012992247 20090703 20090703