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
125712021 12571202 1 I 20120704 20160317 20160719 20160719 EXP DE-BIOGEN-2016BI00209580 BIOGEN 34.18 YR F Y 0.00000 20160719 MD DE DE

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
125712021 12571202 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR 110077A 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
125712021 12571202 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR 110077A 125104 CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125712021 12571202 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125712021 12571202 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125712021 12571202 Caesarean section
125712021 12571202 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
125712021 12571202 1 20070727 20111205 0
125712021 12571202 2 20120102 0