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
126104961 12610496 1 I 20160725 20160801 20160801 EXP US-AMGEN-USASL2016097819 AMGEN 85.00 YR E F Y 0.00000 20160801 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
126104961 12610496 1 PS ENBREL ETANERCEPT 1 Unknown UNK, WEEKLY U 103795 UNKNOWN FORMULATION /wk
126104961 12610496 2 SS FORTEO TERIPARATIDE 1 Unknown UNK 0
126104961 12610496 3 C METHOTREXATE. METHOTREXATE 1 UNK 0
126104961 12610496 4 C FOSAMAX ALENDRONATE SODIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126104961 12610496 1 Rheumatoid arthritis
126104961 12610496 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126104961 12610496 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126104961 12610496 Carbohydrate antigen 125 increased
126104961 12610496 Chills
126104961 12610496 Laboratory test abnormal
126104961 12610496 Malaise
126104961 12610496 Unevaluable event
126104961 12610496 Weight decreased

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

no results found

Therapies reported

no results found