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
101045483 10104548 3 F 20140315 20150923 20140424 20150930 EXP US-SA-2014SA028404 AVENTIS 60.00 YR A M Y 0.00000 20150930 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
101045483 10104548 1 PS AUBAGIO TERIFLUNOMIDE 1 Oral D UNK 202992 14 MG QD
101045483 10104548 2 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 D 0 1 DF QD
101045483 10104548 3 C RELPAX ELETRIPTAN HYDROBROMIDE 1 D 0
101045483 10104548 4 C AZOR AMLODIPINE BESYLATEOLMESARTAN MEDOXOMIL 1 D 0 1 DF QD
101045483 10104548 5 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 4-5 X DAY D 0
101045483 10104548 6 C ALPRAZOLAM. ALPRAZOLAM 1 4-DAY D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101045483 10104548 1 Multiple sclerosis
101045483 10104548 2 Depression
101045483 10104548 4 Blood pressure measurement
101045483 10104548 6 Depression

Outcome of event

Event ID CASEID OUTC COD
101045483 10104548 HO
101045483 10104548 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101045483 10104548 Erythema
101045483 10104548 Gait disturbance
101045483 10104548 Headache
101045483 10104548 Hypersensitivity
101045483 10104548 Impaired driving ability
101045483 10104548 Nausea
101045483 10104548 Progressive multiple sclerosis
101045483 10104548 Pruritus generalised

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
101045483 10104548 1 20140206 20140322 0