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
78488563 7848856 3 F 201102 20110822 20110310 20160708 EXP BR-AMGEN-BRASP2011011790 AMGEN 42.00 YR A M Y 77.00000 KG 20160708 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
78488563 7848856 1 PS etanercept ETANERCEPT 1 Subcutaneous 50 MG, QWK 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
78488563 7848856 2 C EUTHYROX LEVOTHYROXINE SODIUM 1 50 MG, 1X/DAY 0 50 MG
78488563 7848856 3 C EUTHYROX LEVOTHYROXINE SODIUM 1 50 MG, 1X/DAY 0 50 MG QD
78488563 7848856 4 C PANTOZOL /01263202/ 2 20 MG, QD 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
78488563 7848856 1 Rheumatoid arthritis
78488563 7848856 2 Hypothyroidism
78488563 7848856 4 Gastritis

Outcome of event

Event ID CASEID OUTC COD
78488563 7848856 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
78488563 7848856 Food poisoning
78488563 7848856 Immunodeficiency
78488563 7848856 Incorrect product storage
78488563 7848856 Infection
78488563 7848856 Muscle rigidity
78488563 7848856 Myalgia
78488563 7848856 Neutrophil percentage increased
78488563 7848856 Pyrexia
78488563 7848856 Speech disorder

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
78488563 7848856 1 20100903 0
78488563 7848856 3 2005 0
78488563 7848856 4 201010 0