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
100978116 10097811 6 F 20160718 20140423 20160721 EXP BR-AMGEN INC.-BRASP2014029441 AMGEN 49.00 YR A F Y 68.00000 KG 20160721 CN BR BR

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
100978116 10097811 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, WEEKLY Y 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
100978116 10097811 2 C MELOXICAM. MELOXICAM 1 UNK 0
100978116 10097811 3 C MELOXICAM. MELOXICAM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100978116 10097811 1 Rheumatoid arthritis
100978116 10097811 2 Rheumatoid arthritis
100978116 10097811 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
100978116 10097811 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100978116 10097811 Arthralgia
100978116 10097811 Joint swelling
100978116 10097811 Rheumatoid arthritis

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
100978116 10097811 1 20100521 201311 0