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
125581393 12558139 3 F 20160725 20160714 20160804 EXP GB-PFIZER INC-2016333860 PFIZER 49.00 YR F Y 0.00000 20160804 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
125581393 12558139 1 SS DEXAMETHASONE SODIUM PHOSPHATE. DEXAMETHASONE SODIUM PHOSPHATE 1 Oral UNK U 0
125581393 12558139 2 PS EPIRUBICIN HCL EPIRUBICIN HYDROCHLORIDE 1 UNK U 50778
125581393 12558139 3 SS FLUOROURACIL. FLUOROURACIL 1 UNK U 0
125581393 12558139 4 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 UNK U 0
125581393 12558139 5 SS APREPITANT. APREPITANT 1 Oral UNK U 0
125581393 12558139 6 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 UNK U 0
125581393 12558139 7 SS NEULASTA PEGFILGRASTIM 1 UNK U 0
125581393 12558139 8 SS PALONOSETRON HYDROCHLORIDE. PALONOSETRON HYDROCHLORIDE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125581393 12558139 OT
125581393 12558139 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125581393 12558139 Alopecia
125581393 12558139 Application site mass
125581393 12558139 Asthenia
125581393 12558139 Diarrhoea
125581393 12558139 Gastrointestinal viral infection
125581393 12558139 Nausea
125581393 12558139 Neutropenia
125581393 12558139 Vomiting

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

no results found

Therapies reported

no results found