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
125567701 12556770 1 I 20160709 20160711 20160714 20160714 EXP US-AMGEN-USASP2016090050 AMGEN 67.00 YR E F Y 0.00000 20160714 PH 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
125567701 12556770 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 125031 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125567701 12556770 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125567701 12556770 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125567701 12556770 Abdominal pain upper
125567701 12556770 Appetite disorder
125567701 12556770 Arthralgia
125567701 12556770 Bone pain
125567701 12556770 Diarrhoea
125567701 12556770 Ear pain
125567701 12556770 Headache
125567701 12556770 Lymphadenopathy
125567701 12556770 Melaena
125567701 12556770 Myalgia
125567701 12556770 Oropharyngeal pain
125567701 12556770 Pyrexia
125567701 12556770 Snoring
125567701 12556770 Throat irritation

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
125567701 12556770 1 20160708 0