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
126272652 12627265 2 F 2016 20160809 20160805 20160822 EXP GB-CELGENEUS-GBR-2016076542 CELGENE 63.00 YR F Y 0.00000 20160822 OT GB GB

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
126272652 12627265 1 PS ABRAXANE PACLITAXEL 1 Intravenous drip U U 21660 INJECTION FOR INFUSION
126272652 12627265 2 SS APREPITANT. APREPITANT 1 Oral U U 0 UNKNOWN
126272652 12627265 3 SS NEULASTA PEGFILGRASTIM 1 Unknown U 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126272652 12627265 1 Product used for unknown indication
126272652 12627265 2 Product used for unknown indication
126272652 12627265 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126272652 12627265 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126272652 12627265 Back pain
126272652 12627265 Body temperature fluctuation
126272652 12627265 Diarrhoea
126272652 12627265 Fatigue
126272652 12627265 Pain
126272652 12627265 Pain in extremity
126272652 12627265 Pyrexia
126272652 12627265 White blood cell count increased

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

no results found

Therapies reported

no results found