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
127920391 12792039 1 I 20160923 0 20160926 20160926 DIR FDA-CTU 50.00 YR F N 0.00000 20160426 Y PH 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
127920391 12792039 1 PS AMPYRA DALFAMPRIDINE 1 Oral D D VEZS 20181031 0 10 MG Q12H
127920391 12792039 3 C TECFIDERA DIMETHYL FUMARATE 1 0
127920391 12792039 5 C EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 0
127920391 12792039 7 C SANCTURA TROSPIUM CHLORIDE 1 0
127920391 12792039 9 C ADDERALL XR AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 0
127920391 12792039 11 C MOTRIN IBUPROFEN 1 0
127920391 12792039 13 C BACLOFEN. BACLOFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127920391 12792039 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127920391 12792039 Laboratory test abnormal

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

Event ID CASEID RPSR COD
127920391 12792039 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127920391 12792039 1 201208 0