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
126011311 12601131 1 I 20160719 20160728 20160728 PER US-AMGEN-USASP2016094926 AMGEN 56.00 YR A F Y 0.00000 20160728 MD 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
126011311 12601131 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, QWK U 103795 50 MG UNKNOWN FORMULATION /wk
126011311 12601131 2 SS TYLENOL ACETAMINOPHEN 1 Unknown UNK 0
126011311 12601131 3 C GABAPENTIN. GABAPENTIN 1 UNK 0
126011311 12601131 4 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK 0
126011311 12601131 5 C CALCIUM CALCIUM 1 UNK 0
126011311 12601131 6 C VITAMIN D CHOLECALCIFEROL 1 UNK 0
126011311 12601131 7 C VITAMIN B12 CYANOCOBALAMIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126011311 12601131 1 Rheumatoid arthritis
126011311 12601131 2 Myalgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126011311 12601131 Drug ineffective
126011311 12601131 Myalgia

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
126011311 12601131 1 2013 0