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
125867171 12586717 1 I 20160617 0 20160722 20160722 DIR 45.00 YR M N 0.00000 20160721 Y PH 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
125867171 12586717 1 PS AMPYRA DALFAMPRIDINE 1 Oral D D TCNV 20180430 0 10 MG BID
125867171 12586717 3 C SILDENAFIL. SILDENAFIL 1 0
125867171 12586717 5 C HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHENHYDROCODONE BITARTRATE 1 0
125867171 12586717 7 C IBUPROFEN. IBUPROFEN 1 0
125867171 12586717 9 C BACLOFEN. BACLOFEN 1 0
125867171 12586717 11 C NORTRIPTYLINE NORTRIPTYLINE 1 0
125867171 12586717 13 C GABAPENTIN. GABAPENTIN 1 0
125867171 12586717 15 C MUPIROCIN. MUPIROCIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125867171 12586717 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125867171 12586717 B-lymphocyte count increased
125867171 12586717 Laboratory test abnormal

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

Event ID CASEID RPSR COD
125867171 12586717 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125867171 12586717 1 20160617 0