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
127136851 12713685 1 I 201607 20160826 20160904 20160904 EXP US-AMGEN-USASP2016116091 AMGEN 0.00 Y 0.00000 20160904 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
127136851 12713685 1 PS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 125031 SOLUTION FOR INJECTION
127136851 12713685 2 SS ADVIL IBUPROFEN 1 Unknown UNK 0
127136851 12713685 3 SS ADVIL IBUPROFEN 1 0
127136851 12713685 4 C CYTOXAN CYCLOPHOSPHAMIDE 1 UNK 0
127136851 12713685 5 C TAXOTERE DOCETAXEL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127136851 12713685 1 Product used for unknown indication
127136851 12713685 2 Bone pain
127136851 12713685 3 Chest pain

Outcome of event

Event ID CASEID OUTC COD
127136851 12713685 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127136851 12713685 Abdominal pain
127136851 12713685 Bone pain
127136851 12713685 Chest pain
127136851 12713685 Chromaturia
127136851 12713685 Constipation
127136851 12713685 Diarrhoea
127136851 12713685 Fear of death
127136851 12713685 Haemorrhage
127136851 12713685 Haemorrhoids
127136851 12713685 Insomnia
127136851 12713685 Nausea
127136851 12713685 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
127136851 12713685 1 20160627 0