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
125785321 12578532 1 I 20160624 0 20160720 20160720 DIR 44.00 YR F N 0.00000 20160719 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
125785321 12578532 1 PS AMPYRA DALFAMPRIDINE 1 Oral D D TCNV 20180430 0 10 MG Q12H
125785321 12578532 3 C RITUXIMAB RITUXIMAB 1 0
125785321 12578532 5 C DECADRON DEXAMETHASONE 1 0
125785321 12578532 7 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 0
125785321 12578532 9 C ATIVAN LORAZEPAM 1 0
125785321 12578532 11 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0
125785321 12578532 13 C TYLENOL ACETAMINOPHEN 1 0
125785321 12578532 15 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 0
125785321 12578532 17 C PEPCID FAMOTIDINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125785321 12578532 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125785321 12578532 Laboratory test abnormal

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

Event ID CASEID RPSR COD
125785321 12578532 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125785321 12578532 1 201207 0