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
127140761 12714076 1 I 2016 20160826 20160905 20160905 EXP US-AMGEN-USASP2016116521 AMGEN 0.00 Y 0.00000 20160905 CN 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
127140761 12714076 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK UNK, UNK U 125031 UNKNOWN FORMULATION
127140761 12714076 2 C ADVIL IBUPROFEN 1 UNK 0
127140761 12714076 3 C CYTOXAN CYCLOPHOSPHAMIDE 1 UNK 0
127140761 12714076 4 C TAXOTERE DOCETAXEL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127140761 12714076 1 Product used for unknown indication
127140761 12714076 2 Bone pain

Outcome of event

Event ID CASEID OUTC COD
127140761 12714076 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127140761 12714076 Bone pain
127140761 12714076 Chromaturia
127140761 12714076 Diarrhoea
127140761 12714076 Haematochezia
127140761 12714076 Haemorrhoids
127140761 12714076 Seborrhoea

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
127140761 12714076 1 2016 0
127140761 12714076 2 2016 0
127140761 12714076 3 2016 0
127140761 12714076 4 2016 0