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
100264403 10026440 3 F 201311 20140916 20140321 20140930 EXP US-BIOGENIDEC-2014BI026018 BIOGEN 47.00 YR F Y 0.00000 20140930 N CN 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
100264403 10026440 1 PS TYSABRI NATALIZUMAB 1 INTRAVENOUS D 125104 300 MG INTRAVENOUS INFUSION /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100264403 10026440 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
100264403 10026440 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100264403 10026440 Anaemia
100264403 10026440 Blood creatine decreased
100264403 10026440 Constipation
100264403 10026440 Faecal incontinence
100264403 10026440 Gait disturbance
100264403 10026440 Mental impairment
100264403 10026440 Musculoskeletal disorder
100264403 10026440 Neuropathy peripheral
100264403 10026440 Peripheral swelling
100264403 10026440 Renal failure chronic
100264403 10026440 Urinary hesitation
100264403 10026440 Urinary incontinence
100264403 10026440 Urinary retention

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
100264403 10026440 1 20080520 0