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
106781483 10678148 3 F 2013 20160720 20141229 20160726 EXP BR-AMGEN-BRASP2014076414 AMGEN 50.00 YR A F Y 90.00000 KG 20160726 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
106781483 10678148 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, WEEKLY EVERY TUESDAY G94194 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
106781483 10678148 2 SS ENBREL ETANERCEPT 1 Unknown UNK H31342 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
106781483 10678148 3 C TRILAX /01550501/ 2 UNK UNK, QD 0 QD
106781483 10678148 4 C CAPTOPRIL. CAPTOPRIL 1 UNK, DAILY 0 QD
106781483 10678148 5 C HCTZ HYDROCHLOROTHIAZIDE 1 25 MG, UNK 0 25 MG
106781483 10678148 6 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 UNK, DAILY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106781483 10678148 1 Rheumatoid arthritis
106781483 10678148 4 Blood pressure abnormal
106781483 10678148 6 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
106781483 10678148 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106781483 10678148 Apathy
106781483 10678148 Cough
106781483 10678148 Drug ineffective
106781483 10678148 Injection site pain
106781483 10678148 Insomnia
106781483 10678148 Pneumonia

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
106781483 10678148 1 201303 0
106781483 10678148 3 2014 0
106781483 10678148 4 2010 0