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
106787855 10678785 5 F 2015 20160818 20141229 20160829 EXP US-SA-2014SA076253 AVENTIS 61.00 YR A F Y 0.00000 20160829 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
106787855 10678785 1 PS AUBAGIO TERIFLUNOMIDE 1 Oral UNKNOWN 202992 14 MG QD
106787855 10678785 2 SS AMPYRA DALFAMPRIDINE 1 Unknown U UNK 0
106787855 10678785 3 C NITROFURANTOIN. NITROFURANTOIN 1 50 MG 0
106787855 10678785 4 C OXYCODONE OXYCODONE 1 0
106787855 10678785 5 C TYLENOL ACETAMINOPHEN 1 0 TID
106787855 10678785 6 C TYLENOL ACETAMINOPHEN 1 0 3 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106787855 10678785 1 Multiple sclerosis
106787855 10678785 2 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
106787855 10678785 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106787855 10678785 Abdominal pain
106787855 10678785 Anaemia
106787855 10678785 Asthenia
106787855 10678785 Blood sodium decreased
106787855 10678785 Chest pain
106787855 10678785 Drug ineffective
106787855 10678785 Ear pain
106787855 10678785 Hyperkeratosis
106787855 10678785 Multiple sclerosis relapse
106787855 10678785 Muscle atrophy
106787855 10678785 Nausea
106787855 10678785 Nuclear magnetic resonance imaging abnormal
106787855 10678785 Orthosis user
106787855 10678785 Pollakiuria

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
106787855 10678785 1 20131118 0
106787855 10678785 2 20130101 0