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
122617454 12261745 4 F 20160404 20160809 20160413 20160815 EXP PHEH2016US008954 NOVARTIS 69.82 YR F Y 0.00000 20160815 CN COUNTRY NOT SPECIFIED 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
122617454 12261745 1 PS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEKS 1-2: 0.0625 MG (0.25 ML), QOD Y 125290 .062 MG SOLUTION FOR INJECTION
122617454 12261745 2 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEK 3-4, 0.125 MG, (0.5 ML), QOD Y 125290 .125 MG SOLUTION FOR INJECTION
122617454 12261745 3 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEK 5-6, 0.1875 MG, (0.75 ML), QOD Y 125290 .187 MG SOLUTION FOR INJECTION
122617454 12261745 4 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEKS 7+: 0.25 MG, QOD Y 125290 .25 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122617454 12261745 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
122617454 12261745 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122617454 12261745 Asthenia
122617454 12261745 Cardiomyopathy
122617454 12261745 Chest discomfort
122617454 12261745 Coronary artery disease
122617454 12261745 Diarrhoea
122617454 12261745 Dizziness
122617454 12261745 Electrocardiogram abnormal
122617454 12261745 Gait disturbance
122617454 12261745 Hypertension
122617454 12261745 Influenza like illness
122617454 12261745 Insomnia
122617454 12261745 Myocardial infarction
122617454 12261745 Nausea
122617454 12261745 Pain
122617454 12261745 Pallor
122617454 12261745 Palpitations
122617454 12261745 Tinnitus

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
122617454 12261745 1 20160404 0
122617454 12261745 4 20160803 0