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
124886454 12488645 4 F 201608 20160810 20160622 20160817 EXP GB-AMGEN-GBRSP2016077569 AMGEN 66.00 YR E M Y 0.00000 20160817 OT GB GB

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
124886454 12488645 1 PS ARANESP DARBEPOETIN ALFA 1 Unknown 20 MG, UNK U 103951 20 MG SOLUTION FOR INJECTION
124886454 12488645 2 C SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2WK 0 900 MG QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124886454 12488645 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124886454 12488645 OT
124886454 12488645 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124886454 12488645 Abdominal distension
124886454 12488645 Abdominal pain upper
124886454 12488645 Chromaturia
124886454 12488645 Constipation
124886454 12488645 Decreased appetite
124886454 12488645 Dyspnoea
124886454 12488645 Fatigue
124886454 12488645 Haemoglobin abnormal
124886454 12488645 Haemoglobin decreased
124886454 12488645 Hiccups
124886454 12488645 Hypertension
124886454 12488645 Insomnia
124886454 12488645 Malaise
124886454 12488645 Muscle spasms
124886454 12488645 Nausea
124886454 12488645 Oropharyngeal pain
124886454 12488645 Vomiting
124886454 12488645 Vomiting projectile

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
124886454 12488645 1 20160603 0