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
82835952 8283595 2 F 201107 20120224 20111122 20120426 PER PHHY2011US68101 NOVARTIS 33.00 YR F N 0.00000 20120306 CN 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
82835952 8283595 1 PS GILENYA 1 ORAL S0007B 20121231 22527 0.5 MG QD
82835952 8283595 2 C HYDROCODONE W/APAP (HYDROCODONE, PARACETAMOL) 2 0
82835952 8283595 3 C ALPRAZOLAM 1 0
82835952 8283595 4 C CYCLOBENZAPRINE 1 0
82835952 8283595 5 C ZOLPIDEM 1 0
82835952 8283595 6 C CITALOPRAM HYDROBROMIDE 1 0
82835952 8283595 8 C BACLOFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
82835952 8283595 1 MULTIPLE SCLEROSIS

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
82835952 8283595 Asthenia
82835952 8283595 Memory impairment
82835952 8283595 Ovarian disorder
82835952 8283595 Visual impairment
82835952 8283595 Weight increased

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

Event ID CASEID RPSR COD
82835952 8283595 CSM

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
82835952 8283595 1 20110527 0