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
125032982 12503298 2 F 2016 20160704 20160628 20160713 EXP GB-MHRA-ADR 23519928 GB-ACCORD-041784 ACCORD 42.00 YR F Y 0.00000 20160713 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
125032982 12503298 1 PS DOCETAXEL. DOCETAXEL 1 3 CYCLE U 201195
125032982 12503298 2 SS FLUOROURACIL. FLUOROURACIL 1 U 40743 Q3W
125032982 12503298 3 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 U 11811
125032982 12503298 4 SS ONDANSETRON ONDANSETRON 1 U 206846
125032982 12503298 5 SS EPIRUBICIN EPIRUBICIN 1 U 2147483647
125032982 12503298 6 SS NEULASTA PEGFILGRASTIM 1 Subcutaneous 6 MG, 24 HOURS AFTER CHEMOTHERAPY U 0 6 MG
125032982 12503298 7 SS APREPITANT. APREPITANT 1 Oral 80 MG, ONCE A DAY (TAKEN ON DAY 2 AND 3 AFTER CHEMOTHERAPY) U 0 80 MG QD
125032982 12503298 8 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral 2 MG, ONCE DAILY, 3 DAYS U 0 2 MG QD
125032982 12503298 9 SS LEVOMEPROMAZINE LEVOMEPROMAZINE 1 U 0
125032982 12503298 10 SS CYCLOPHOSPHAMIDE/CYCLOPHOSPHAMIDE MONOHYDRATE CYCLOPHOSPHAMIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125032982 12503298 1 Product used for unknown indication
125032982 12503298 2 Product used for unknown indication
125032982 12503298 3 Product used for unknown indication
125032982 12503298 4 Product used for unknown indication
125032982 12503298 5 Product used for unknown indication
125032982 12503298 6 Product used for unknown indication
125032982 12503298 7 Product used for unknown indication
125032982 12503298 8 Product used for unknown indication
125032982 12503298 9 Product used for unknown indication
125032982 12503298 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125032982 12503298 OT
125032982 12503298 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125032982 12503298 Arthralgia
125032982 12503298 Constipation
125032982 12503298 Decreased appetite
125032982 12503298 Deep vein thrombosis
125032982 12503298 Fatigue
125032982 12503298 Oral pain
125032982 12503298 Pain
125032982 12503298 Vascular pain

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

no results found

Therapies reported

no results found