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
126483741 12648374 1 I 2016 20160809 20160812 20160812 EXP GB-009507513-1608GBR005817 MERCK 63.00 YR F Y 0.00000 20160812 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
126483741 12648374 1 PS EMEND APREPITANT 1 Oral UNK U U 21549 CAPSULE
126483741 12648374 2 SS ABRAXANE PACLITAXEL 1 Intravenous drip UNK U U 0 INTRAVENOUS INFUSION
126483741 12648374 3 SS NEULASTA PEGFILGRASTIM 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126483741 12648374 1 Product used for unknown indication
126483741 12648374 2 Product used for unknown indication
126483741 12648374 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126483741 12648374 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126483741 12648374 Back pain
126483741 12648374 Body temperature fluctuation
126483741 12648374 Diarrhoea
126483741 12648374 Fatigue
126483741 12648374 Pain
126483741 12648374 Pain in extremity
126483741 12648374 Pyrexia
126483741 12648374 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