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
126173911 12617391 1 I 20160729 20160803 20160803 PER PHEH2016US019296 NOVARTIS 0.00 M Y 0.00000 20160803 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
126173911 12617391 1 PS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEKS1-2: 0.0625 MG (0.25 ML), QOD 125290 .25 ML SOLUTION FOR INJECTION
126173911 12617391 2 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEKS 3-4: 0.125 MG (0.5 ML), QOD 125290 .5 ML SOLUTION FOR INJECTION
126173911 12617391 3 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEKS 5-6: 0.1875 MG (0.75 ML), QOD 125290 .75 ML SOLUTION FOR INJECTION
126173911 12617391 4 SS EXTAVIA INTERFERON BETA-1B 1 Subcutaneous WEEKS 7+: 0.25 MG (1 ML), QOD 125290 1 ML SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126173911 12617391 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126173911 12617391 Burning sensation
126173911 12617391 Hypoaesthesia
126173911 12617391 Muscle tightness
126173911 12617391 Paraesthesia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found