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
118367395 11836739 5 F 201512 20160902 20151215 20160909 EXP US-BIOGEN-2015BI00160830 BIOGEN 58.55 YR M Y 0.00000 20160909 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
118367395 11836739 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) P80049 125104 CONCENTRATE FOR SOLUTION FOR INFUSION
118367395 11836739 2 C Atorvastatin ATORVASTATIN 1 Unknown 0 40 MG TABLETS QD
118367395 11836739 3 C TRAMADOL. TRAMADOL 1 Unknown 0 25 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118367395 11836739 1 Multiple sclerosis
118367395 11836739 2 Product used for unknown indication
118367395 11836739 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118367395 11836739 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118367395 11836739 Ischaemic cerebral infarction
118367395 11836739 Leukocytosis
118367395 11836739 Pneumonia
118367395 11836739 Pyrexia
118367395 11836739 Tachycardia

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
118367395 11836739 1 20070126 0