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
102096742 10209674 2 F 20150619 20140602 20150630 EXP US-BIOGENIDEC-2014BI049382 BIOGEN 0.00 F Y 0.00000 20150630 N 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
102096742 10209674 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular D 103628 30 UG /wk
102096742 10209674 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular D 103628 30 UG SOLUTION FOR INJECTION /wk
102096742 10209674 3 SS AVONEX INTERFERON BETA-1A 1 Intramuscular D 103628 7 UG /wk
102096742 10209674 4 SS AVONEX INTERFERON BETA-1A 1 Intramuscular D 103628 30 UG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102096742 10209674 1 Multiple sclerosis
102096742 10209674 2 Multiple sclerosis
102096742 10209674 3 Multiple sclerosis
102096742 10209674 4 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
102096742 10209674 HO
102096742 10209674 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
102096742 10209674 Abasia
102096742 10209674 Blindness
102096742 10209674 Cardiac failure congestive
102096742 10209674 Coordination abnormal
102096742 10209674 Foot fracture
102096742 10209674 General physical health deterioration
102096742 10209674 General symptom
102096742 10209674 Headache
102096742 10209674 Loss of consciousness
102096742 10209674 Mobility decreased
102096742 10209674 Muscle atrophy
102096742 10209674 Muscle disorder
102096742 10209674 Muscle spasms
102096742 10209674 Myoclonic epilepsy
102096742 10209674 Osteoporosis
102096742 10209674 Peripheral swelling
102096742 10209674 Renal impairment
102096742 10209674 Seizure
102096742 10209674 Sensory disturbance
102096742 10209674 Sleep apnoea syndrome
102096742 10209674 Tremor
102096742 10209674 Urticaria

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
102096742 10209674 2 20060311 20070318 0
102096742 10209674 3 20140523 0