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
125233621 12523362 1 I 20160624 20160702 20160702 EXP US-AMGEN-USASP2016082903 AMGEN 67.00 YR E M Y 0.00000 20160702 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
125233621 12523362 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 125031 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125233621 12523362 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125233621 12523362 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125233621 12523362 Activities of daily living impaired
125233621 12523362 Application site haemorrhage
125233621 12523362 Application site pain
125233621 12523362 Arthritis
125233621 12523362 Asthenia
125233621 12523362 Fatigue
125233621 12523362 Joint range of motion decreased
125233621 12523362 Musculoskeletal pain
125233621 12523362 Myalgia
125233621 12523362 Neuropathy peripheral
125233621 12523362 Pain in extremity
125233621 12523362 Pneumonia
125233621 12523362 Sleep disorder

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found