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
127123801 12712380 1 I 2015 20160226 20160902 20160902 EXP CA-PFIZER INC-2016130276 PFIZER 38.00 YR F Y 0.00000 20160902 MD CA CA

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
127123801 12712380 1 SS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, WEEKLY N 0 50 MG /wk
127123801 12712380 2 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 150 MG, 1X/DAY N 20699 150 MG PROLONGED-RELEASE CAPSULE QD
127123801 12712380 3 SS LEFLUNOMIDE. LEFLUNOMIDE 1 UNK U 0 TABLET
127123801 12712380 4 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 300 MG, 1X/DAY 0 300 MG TABLET QD
127123801 12712380 5 C REACTINE CETIRIZINE HYDROCHLORIDE 1 10 MG, 1X/DAY 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127123801 12712380 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127123801 12712380 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127123801 12712380 Anaphylactic shock
127123801 12712380 Arthritis
127123801 12712380 Drug effect incomplete
127123801 12712380 Drug hypersensitivity
127123801 12712380 Drug ineffective
127123801 12712380 Drug intolerance
127123801 12712380 Insomnia
127123801 12712380 Pain
127123801 12712380 Rash

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
127123801 12712380 1 201602 0