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
125615873 12561587 3 F 201606 20160802 20160715 20160811 EXP GB-MHRA-009507513-1606GBR007583 GB-FRESENIUS KABI-FK201604351 FRESENIUS KABI 69.00 YR F Y 0.00000 20160811 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
125615873 12561587 1 PS ONDANSETRON (MANUFACTURER UNKNOWN) ONDANSETRON 1 Intravenous (not otherwise specified) U UNKNOWN 76972 8 MG UNKNOWN
125615873 12561587 2 SS EPIRUBICIN (Manufacturer unknown) EPIRUBICIN 1 Intravenous (not otherwise specified) U UNKNOWN 65411 126 MG UNKNOWN QD
125615873 12561587 3 SS EPIRUBICIN (Manufacturer unknown) EPIRUBICIN 1 Intravenous (not otherwise specified) U UNKNOWN 65411 UNKNOWN /cycle
125615873 12561587 4 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Intravenous (not otherwise specified) 0 9 MG UNKNOWN QD
125615873 12561587 5 SS DEXAMETHASONE. DEXAMETHASONE 1 Intravenous (not otherwise specified) 0 8 MG UNKNOWN QD
125615873 12561587 6 SS EMEND APREPITANT 1 Oral 0 125 MG UNKNOWN QD
125615873 12561587 7 SS FLUOROURACIL. FLUOROURACIL 1 Intravenous (not otherwise specified) 0 UNKNOWN
125615873 12561587 8 SS FLUOROURACIL. FLUOROURACIL 1 0
125615873 12561587 9 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 Unknown 0 UNKNOWN QD
125615873 12561587 10 SS NEULASTA PEGFILGRASTIM 1 Subcutaneous 0 6 MG UNKNOWN QD
125615873 12561587 11 SS NEULASTA PEGFILGRASTIM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125615873 12561587 1 Product used for unknown indication
125615873 12561587 2 Breast cancer
125615873 12561587 3 Product used for unknown indication
125615873 12561587 4 Product used for unknown indication
125615873 12561587 5 Product used for unknown indication
125615873 12561587 6 Product used for unknown indication
125615873 12561587 7 Breast cancer
125615873 12561587 8 Product used for unknown indication
125615873 12561587 9 Product used for unknown indication
125615873 12561587 10 Breast cancer
125615873 12561587 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125615873 12561587 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125615873 12561587 Alopecia
125615873 12561587 Body temperature abnormal
125615873 12561587 Condition aggravated
125615873 12561587 Cough
125615873 12561587 Diarrhoea
125615873 12561587 Dyspnoea
125615873 12561587 Ear pain
125615873 12561587 Eating disorder
125615873 12561587 Fatigue
125615873 12561587 Feeling abnormal
125615873 12561587 Glossodynia
125615873 12561587 Headache
125615873 12561587 Hypophagia
125615873 12561587 Intercepted drug administration error
125615873 12561587 Lethargy
125615873 12561587 Lower respiratory tract infection
125615873 12561587 Malaise
125615873 12561587 Nausea
125615873 12561587 Odynophagia
125615873 12561587 Oral pain
125615873 12561587 Oropharyngeal pain
125615873 12561587 Pharyngeal erythema
125615873 12561587 Productive cough
125615873 12561587 Sputum discoloured
125615873 12561587 Vomiting

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125615873 12561587 2 20160608 0
125615873 12561587 4 20160608 0
125615873 12561587 7 20160608 0
125615873 12561587 10 20160608 0