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
78136744 7813674 4 F 20110130 20121226 20110216 20121231 EXP US-BIOGENIDEC-2011BI004951 BIOGEN 1.00 DY M Y 3.00000 KG 20121231 OT 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
78136744 7813674 1 PS TYSABRI 1 TRANSPLACENTAL D UNK 125104 300 MG Intravenous infusion /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
78136744 7813674 1 Maternal exposure timing unspecified

Outcome of event

Event ID CASEID OUTC COD
78136744 7813674 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
78136744 7813674 Limb malformation

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
78136744 7813674 1 20061213 20100604 0