The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
74318526 7431852 6 F 200701 20131219 20100624 20131231 PER US-BIOGENIDEC-2010BI020604 BIOGEN 45.07 YR F Y 0.00000 20131231 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
74318526 7431852 1 PS TYSABRI 1 INTRAVENOUS D 125104 300 MG INTRAVENOUS INFUSION /month
74318526 7431852 2 SS TYSABRI 1 INTRAVENOUS D 125104 300 MG INTRAVENOUS INFUSION /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
74318526 7431852 1 Multiple sclerosis
74318526 7431852 2 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
74318526 7431852 Amnesia
74318526 7431852 Chills
74318526 7431852 Colitis ulcerative
74318526 7431852 Diarrhoea
74318526 7431852 Gastroenteritis salmonella
74318526 7431852 Hypersensitivity
74318526 7431852 Nausea
74318526 7431852 Poor venous access
74318526 7431852 Rash macular
74318526 7431852 Salmonellosis
74318526 7431852 Tendonitis

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
74318526 7431852 1 20061219 20100329 0
74318526 7431852 2 20061219 0