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
126476861 12647686 1 I 20160706 0 20160811 20160811 DIR 51.00 YR F N 0.00000 20160809 N 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
126476861 12647686 1 PS ENBREL ETANERCEPT 1 Subcutaneous D D 1065295 20181130 0 50 MG QW
126476861 12647686 2 SS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Y D 0
126476861 12647686 4 C NITROFURANTIN NITROFURANTOIN 1 0
126476861 12647686 6 C AMOX/KCLAV 2 0
126476861 12647686 8 C DICLOFENAC DICLOFENAC 1 0
126476861 12647686 10 C CEPHALEXIN. CEPHALEXIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126476861 12647686 1 Psoriasis
126476861 12647686 2 Nausea

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126476861 12647686 Erythema
126476861 12647686 Headache
126476861 12647686 Rash
126476861 12647686 Refusal of treatment by patient

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

Event ID CASEID RPSR COD
126476861 12647686 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126476861 12647686 1 20140626 0
126476861 12647686 2 20160706 0