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
4364108 4144429 I 4364108-1 20040405 20040513 20040525 EXP DE-BRISTOL-MYERS SQUIBB COMPANY-12585527 BRISTOL-MYERS SQUIBB COMPANY 57 YR F Y 77 KG 20040525 OT

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
4364108 1004887103 PS IFOSFAMIDE 1 INTRAVENOUS THERAPY DATES: 03-APR TO 05-APR-2004; WITHDRAWN ON 08-APR-2004
4364108 1004887104 SS CAELYX 2 INTRAVENOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
4364108 1004887103 SARCOMA
4364108 1004887104 SARCOMA

Outcome of event

Event ID OUTC COD
4364108 HO
4364108 OT

Reactions reported

Event ID PT
4364108 PSYCHOTIC DISORDER
4364108 TOXIC INDUCED ENCEPHALOPATHY

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

Event ID RPSR COD
4364108 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4364108 1004887103 20040403 20040405
4364108 1004887104 20040403 20040403