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
5127243 5903287 F 1 5127243-6 20050901 20060929 20061010 EXP 2005BI017679 BIOGEN IDEC INC. 45 YR M N 120 KG 20061009 MD 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
5127243 1007757411 PS AVONEX 1 INTRAMUSCULAR 30 UG; QW; IM D D

Indications of drugs used

Event ID DRUG SEQ INDI PT
5127243 1007757411 MULTIPLE SCLEROSIS

Outcome of event

Event ID OUTC COD
5127243 HO

Reactions reported

Event ID PT
5127243 ALCOHOLISM
5127243 ANXIETY
5127243 ASPARTATE AMINOTRANSFERASE INCREASED
5127243 BRAIN NATRIURETIC PEPTIDE INCREASED
5127243 BUNDLE BRANCH BLOCK LEFT
5127243 CARDIAC FAILURE ACUTE
5127243 CARDIOMEGALY
5127243 CARDIOMYOPATHY
5127243 GAMMA-GLUTAMYLTRANSFERASE INCREASED
5127243 HEPATOJUGULAR REFLUX
5127243 INSOMNIA
5127243 PRURIGO
5127243 RASH ERYTHEMATOUS
5127243 SINUS TACHYCARDIA
5127243 SKIN LESION
5127243 VENTRICULAR HYPOKINESIA
5127243 WEIGHT INCREASED

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

Event ID RPSR COD
5127243 FGN
5127243 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5127243 1007757411 20031001 20050901