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
127716041 12771604 1 I 2016 20160707 20160922 20160922 PER US-AMGEN-USASP2016089594 AMGEN 55.00 YR A F Y 0.00000 20160922 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
127716041 12771604 1 PS NEUPOGEN FILGRASTIM 1 Unknown UNK UNK, 3 TIMES/WK 103353 SOLUTION FOR INJECTION TIW
127716041 12771604 2 SS NEULASTA PEGFILGRASTIM 1 Unknown UNK Y 0 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127716041 12771604 1 White blood cell count decreased
127716041 12771604 2 White blood cell count decreased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127716041 12771604 Bone pain
127716041 12771604 Cough
127716041 12771604 Implant site erythema
127716041 12771604 Implant site induration
127716041 12771604 Implant site warmth
127716041 12771604 Inflammation
127716041 12771604 Paraesthesia
127716041 12771604 Pyrexia
127716041 12771604 White blood cell count increased

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
127716041 12771604 2 201604 0