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
124857162 12485716 2 F 20160519 20160705 20160621 20160715 EXP US-BAYER-2016-113521 BAYER 55.00 YR A F Y 0.00000 20160715 OT 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
124857162 12485716 1 PS BETASERON INTERFERON BETA-1B 1 Y 103471 POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
124857162 12485716 2 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 0H105V 0 10 MG BID
124857162 12485716 3 SS TECFIDERA DIMETHYL FUMARATE 1 UNK UNK, UNK 0
124857162 12485716 4 C BACLOFEN. BACLOFEN 1 0
124857162 12485716 5 C VITAMIN D [ERGOCALCIFEROL] 2 0
124857162 12485716 6 C VITAMIN D3 CHOLECALCIFEROL 1 0
124857162 12485716 7 C CALCIUM CALCIUM 1 0
124857162 12485716 8 C RANITIDINE. RANITIDINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124857162 12485716 1 Product used for unknown indication
124857162 12485716 2 Multiple sclerosis
124857162 12485716 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124857162 12485716 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124857162 12485716 Dizziness
124857162 12485716 Lymphocyte count decreased
124857162 12485716 Ovarian cancer
124857162 12485716 Supraventricular tachycardia
124857162 12485716 Uterine cancer
124857162 12485716 White blood cell count decreased

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
124857162 12485716 2 201010 201101 0