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
80096672 8009667 2 F 20110611 20121217 20110627 20121231 PER US-BIOGENIDEC-2011BI022662 BIOGEN 47.00 YR F Y 0.00000 20121231 CN 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
80096672 8009667 1 PS AVONEX 1 INTRAMUSCULAR D 103628 30 UG Solution for injection /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
80096672 8009667 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
80096672 8009667 Abscess oral
80096672 8009667 Adverse drug reaction
80096672 8009667 Chills
80096672 8009667 Feeling abnormal
80096672 8009667 Headache
80096672 8009667 Influenza like illness
80096672 8009667 Myalgia
80096672 8009667 Nausea
80096672 8009667 Oral pain
80096672 8009667 Pyrexia
80096672 8009667 Tooth abscess

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
80096672 8009667 1 20110611 20110625 0