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
125526722 12552672 2 F 20160725 20160713 20160804 EXP GB-PFIZER INC-2016330161 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
125526722 12552672 1 SS DEXAMETHASONE SODIUM PHOSPHATE. DEXAMETHASONE SODIUM PHOSPHATE 1 Oral UNK U 0
125526722 12552672 2 PS EPIRUBICIN HCL EPIRUBICIN HYDROCHLORIDE 1 UNK U 50778
125526722 12552672 3 SS FLUOROURACIL. FLUOROURACIL 1 UNK U 0
125526722 12552672 4 SS ALOXI PALONOSETRON HYDROCHLORIDE 1 UNK U 0
125526722 12552672 5 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 UNK U 0
125526722 12552672 6 SS APREPITANT. APREPITANT 1 Oral UNK U 0
125526722 12552672 7 SS NEULASTA PEGFILGRASTIM 1 UNK U 0
125526722 12552672 8 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125526722 12552672 OT
125526722 12552672 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125526722 12552672 Alopecia
125526722 12552672 Asthenia
125526722 12552672 Diarrhoea
125526722 12552672 Gastroenteritis
125526722 12552672 Injection site mass
125526722 12552672 Nausea
125526722 12552672 Neutropenia
125526722 12552672 Vomiting

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

no results found

Therapies reported

no results found