The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5159522 6165980 F 1 5159522-0 20060401 20061102 20061120 EXP JP-2006-030239 BERLEX INC. 54 YR M N 20061115 MD JAPAN

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5159522 1007888279 PS BETAFERON (INTERFERON BETA -1B) INJECTION, 250UG 2 SUBCUTANEOUS 8 MIU, EVERY 2D, SUBCUTANEOUS D D
5159522 1007918771 SS PREDONINE (PREDNISOLONE) TABLET, 5MG 2 ORAL 10 MG, 1X/DAY, ORAL U U
5159522 1007918775 C IMURAN (AZATHIOPRINE) TABLET 2
5159522 1007918776 C PLETAAL (CILOSTAZOL), TABLET 2
5159522 1007918778 C TOLEDOMIN (MILNACIPRAN HYDROCHLORIDE) TABLET 2
5159522 1007918779 C TEGRETAL (CARBAMAZEPINE) TABLET 2
5159522 1007918781 C GASTER D (FAMOTIDINE) TABLET 2
5159522 1007918783 C CLONAZEPAM 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5159522 1007888279 MULTIPLE SCLEROSIS
5159522 1007918771 MULTIPLE SCLEROSIS

Outcome of event

Event ID OUTC COD
5159522 HO

Reactions reported

Event ID PT
5159522 DRUG INEFFECTIVE
5159522 GAIT DISTURBANCE
5159522 HEMIPLEGIA
5159522 LACUNAR INFARCTION
5159522 VISUAL DISTURBANCE

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

Event ID RPSR COD
5159522 FGN
5159522 HP
5159522 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5159522 1007888279 20051001
5159522 1007918771 20030501