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
126489971 12648997 1 I 2016 20160805 20160812 20160812 EXP US-AMGEN-USASP2016102547 AMGEN 39.00 YR A F Y 0.00000 20160812 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
126489971 12648997 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 125031 SOLUTION FOR INJECTION
126489971 12648997 2 SS TYLENOL ACETAMINOPHEN 1 Unknown UNK 0
126489971 12648997 3 SS SODIUM CHLORIDE. SODIUM CHLORIDE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126489971 12648997 1 Product used for unknown indication
126489971 12648997 2 Pyrexia
126489971 12648997 3 Hypotension

Outcome of event

Event ID CASEID OUTC COD
126489971 12648997 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126489971 12648997 Abdominal pain upper
126489971 12648997 Diarrhoea
126489971 12648997 Hypotension
126489971 12648997 Peripheral swelling
126489971 12648997 Pyrexia
126489971 12648997 Swelling face
126489971 12648997 Vomiting
126489971 12648997 White blood cell count decreased

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
126489971 12648997 1 2016 0