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
125213392 12521339 2 F 20160630 20160701 20160714 EXP US-ACORDA-ACO_123778_2016 ACORDA 0.00 F Y 0.00000 20160714 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
125213392 12521339 1 PS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 0000079809 22250 10 MG TABLET BID
125213392 12521339 2 SS AMPYRA DALFAMPRIDINE 1 22250 TABLET
125213392 12521339 3 C VITAMIN D CHOLECALCIFEROL 1 U 0
125213392 12521339 4 C Senna Maximum Strength 2 U 0
125213392 12521339 5 C PAMELOR NORTRIPTYLINE HYDROCHLORIDE 1 U 0
125213392 12521339 6 C ESTRACE ESTRADIOL 1 U 0
125213392 12521339 7 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 U 0
125213392 12521339 8 C Calcium Citrate + D 2 U 0
125213392 12521339 9 C FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 U 0
125213392 12521339 10 C TYSABRI NATALIZUMAB 1 U 0
125213392 12521339 11 C BACLOFEN. BACLOFEN 1 U 0
125213392 12521339 12 C Vitamin B-12 CR 2 U 0
125213392 12521339 13 C MELOXICAM. MELOXICAM 1 U 0
125213392 12521339 14 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 U 0
125213392 12521339 15 C Methadone hcl METHADONE HYDROCHLORIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125213392 12521339 1 Multiple sclerosis
125213392 12521339 2 Gait disturbance
125213392 12521339 3 Product used for unknown indication
125213392 12521339 4 Product used for unknown indication
125213392 12521339 5 Product used for unknown indication
125213392 12521339 6 Product used for unknown indication
125213392 12521339 7 Product used for unknown indication
125213392 12521339 8 Product used for unknown indication
125213392 12521339 9 Product used for unknown indication
125213392 12521339 10 Product used for unknown indication
125213392 12521339 11 Product used for unknown indication
125213392 12521339 12 Product used for unknown indication
125213392 12521339 13 Product used for unknown indication
125213392 12521339 14 Product used for unknown indication
125213392 12521339 15 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125213392 12521339 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125213392 12521339 Condition aggravated
125213392 12521339 Intervertebral disc disorder

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
125213392 12521339 1 2011 0