The Safety Rates Drug Report

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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
82899172 8289917 2 F 201104 20120123 20111122 20120426 PER PHHY2011US61565 NOVARTIS 57.00 YR F N 0.00000 20120306 MD 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
82899172 8289917 1 PS GILENYA 1 ORAL 0.5 MG, QD, ORAL N D 22527
82899172 8289917 2 C FIORICET (BUTALBITAL, CAFFEINE, PARACETAMOL) TABLET 2 0
82899172 8289917 3 C LORAZEPAM 1 0
82899172 8289917 4 C NEXIUM 1 0
82899172 8289917 5 C PERCOCET 1 0
82899172 8289917 6 C OXYBUTYNIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
82899172 8289917 1 MULTIPLE SCLEROSIS

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
82899172 8289917 Aspiration
82899172 8289917 Balance disorder
82899172 8289917 Dysphagia
82899172 8289917 Hypoacusis
82899172 8289917 White blood cell count increased

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

Event ID CASEID RPSR COD
82899172 8289917 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
82899172 8289917 1 20110215 20110802 0