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
124997303 12499730 3 F 20160825 20160627 20160905 EXP PT-BIOGEN-2016BI00252545 BIOGEN 0.00 F Y 0.00000 20160905 MD PT PT

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
124997303 12499730 1 PS TECFIDERA DIMETHYL FUMARATE 1 Oral 204063 PROLONGED-RELEASE CAPSULE
124997303 12499730 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 11469 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
124997303 12499730 3 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown 0 UNKNOWN
124997303 12499730 4 C CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown 0 UNKNOWN
124997303 12499730 5 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Intravenous (not otherwise specified) 0 UNKNOWN
124997303 12499730 6 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Oral 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124997303 12499730 1 Product used for unknown indication
124997303 12499730 2 Product used for unknown indication
124997303 12499730 3 Product used for unknown indication
124997303 12499730 4 Product used for unknown indication
124997303 12499730 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124997303 12499730 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124997303 12499730 Multiple sclerosis

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
124997303 12499730 1 201603 0
124997303 12499730 2 201407 20151204 0
124997303 12499730 3 201605 0