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
126202281 12620228 1 I 20160721 20160803 20160803 EXP GB-TEVA-679679ACC TEVA 50.00 YR F Y 0.00000 20160804 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
126202281 12620228 1 PS EPIRUBICIN EPIRUBICIN 1 U U 65331
126202281 12620228 2 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 U U 70184
126202281 12620228 3 SS APREPITANT. APREPITANT 1 U U 0
126202281 12620228 4 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 U U 0
126202281 12620228 5 SS DEXAMETHASONE. DEXAMETHASONE 1 U U 0
126202281 12620228 6 SS FLUOROURACIL. FLUOROURACIL 1 U U 0
126202281 12620228 7 SS NEULASTA PEGFILGRASTIM 1 U U 0
126202281 12620228 8 SS PALONOSETRON PALONOSETRON 1 U U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126202281 12620228 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126202281 12620228 Abdominal discomfort
126202281 12620228 Alopecia
126202281 12620228 Asthenia
126202281 12620228 Diarrhoea
126202281 12620228 Nausea
126202281 12620228 Neutropenia
126202281 12620228 Vomiting

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

no results found

Therapies reported

no results found