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
4303668 4029730 F 2 4303668-3 20030101 20040206 20040223 EXP 701234 BIOGEN IDEC 49 YR F N 130 LBS 20040220 MD

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
4303668 1004650063 PS AMEVIVE 1 INTRAMUSCULAR 15 MG QW IM D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
4303668 1004650063 PSORIASIS

Outcome of event

Event ID OUTC COD
4303668 OT

Reactions reported

Event ID PT
4303668 ALANINE AMINOTRANSFERASE INCREASED
4303668 ASPARTATE AMINOTRANSFERASE INCREASED
4303668 CONDITION AGGRAVATED
4303668 GAMMA-GLUTAMYLTRANSFERASE INCREASED
4303668 HEPATIC STEATOSIS
4303668 HYPERLIPIDAEMIA
4303668 IATROGENIC INJURY
4303668 PRURITUS
4303668 PSORIASIS
4303668 THERMAL BURN
4303668 TREMOR
4303668 VOMITING

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

Event ID RPSR COD
4303668 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4303668 1004650063 20030506 20030101