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
125840351 12584035 1 I 20160714 20160722 20160722 EXP GB-MYLANLABS-2016M1029629 MYLAN 0.00 Y 0.00000 20160722 CN 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
125840351 12584035 1 PS EPIRUBICIN EPIRUBICIN 1 UNK U U 91599
125840351 12584035 2 SS ONDANSETRON ONDANSETRON 1 UNK U U 0
125840351 12584035 3 SS APREPITANT. APREPITANT 1 UNK U U 0
125840351 12584035 4 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 UNK U U 0
125840351 12584035 5 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 UNK U U 0
125840351 12584035 6 SS NEULASTA PEGFILGRASTIM 1 UNK U U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125840351 12584035 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125840351 12584035 Alopecia
125840351 12584035 Fatigue
125840351 12584035 Headache
125840351 12584035 Lower respiratory tract infection
125840351 12584035 Nausea

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

no results found

Therapies reported

no results found