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
126008251 12600825 1 I 20160524 20151021 20160727 20160727 EXP US-BIOGEN-2015BI143077 BIOGEN 24.92 YR F Y 73.09000 KG 20160727 MD COUNTRY NOT SPECIFIED 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
126008251 12600825 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
126008251 12600825 2 C Oxycodone OXYCODONE 1 Unknown 0 UNKNOWN
126008251 12600825 3 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 Unknown 0 UNKNOWN
126008251 12600825 4 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 0
126008251 12600825 5 C DEPAKOTE DIVALPROEX SODIUM 1 Unknown 0 UNKNOWN
126008251 12600825 6 C Td (Tetanus, Diphtheria) 2 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126008251 12600825 1 Multiple sclerosis
126008251 12600825 2 Product used for unknown indication
126008251 12600825 3 Anxiety
126008251 12600825 4 Depression
126008251 12600825 5 Product used for unknown indication
126008251 12600825 6 Immunisation

Outcome of event

Event ID CASEID OUTC COD
126008251 12600825 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126008251 12600825 Breech presentation
126008251 12600825 Maternal exposure during pregnancy

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
126008251 12600825 1 20150810 20150810 0
126008251 12600825 6 20160423 0