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
121267693 12126769 3 F 2015 20160826 20160229 20160902 EXP US-BIOGEN-2015BI156357 BIOGEN 0.00 M Y 74.91000 KG 20160902 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
121267693 12126769 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
121267693 12126769 2 C AMPYRA DALFAMPRIDINE 1 Unknown 0 10 MG UNKNOWN BID
121267693 12126769 3 C atorvastatin ATORVASTATIN 1 Unknown 0 40 MG UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121267693 12126769 1 Multiple sclerosis
121267693 12126769 2 Multiple sclerosis
121267693 12126769 3 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
121267693 12126769 OT
121267693 12126769 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
121267693 12126769 Appendicitis perforated
121267693 12126769 Fall
121267693 12126769 Non-small cell lung cancer
121267693 12126769 Pneumonia

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
121267693 12126769 1 20070807 20151020 0