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
6039519 7084274 I 6039519-9 20081219 20081219 20090106 EXP 3005078272-2009-0001 CELL THERAPY LABORATORY 6 M N 20 KG 20090102 OT UNITED STATES

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
6039519 1010993914 PS HEMATOPOETIC PROGENITOR CELLS HUMAN 1 INTRAVENOUS DRIP 728ML; IV DRIP D D SC01409 20081222

Indications of drugs used

Event ID DRUG SEQ INDI PT
6039519 1010993914 TRANSPLANT FAILURE

Outcome of event

Event ID OUTC COD
6039519 OT

Reactions reported

Event ID PT
6039519 CHILLS
6039519 DYSPNOEA
6039519 HALLUCINATION
6039519 HYPERTENSION
6039519 INFUSION RELATED REACTION
6039519 NAUSEA
6039519 OXYGEN SATURATION DECREASED
6039519 PYREXIA
6039519 TACHYCARDIA
6039519 TACHYPNOEA
6039519 VOMITING

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

Event ID RPSR COD
6039519 HP
6039519 UF

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6039519 1010993914 20081219