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
1123232812 11232328 12 F 201504 20160920 20150701 20160923 EXP GB-ROCHE-1592679 ROCHE 72.20 YR F Y 0.00000 20160923 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
1123232812 11232328 1 PS Pertuzumab PERTUZUMAB 1 Intravenous (not otherwise specified) 125409 420 MG SOLUTION FOR INFUSION Q3W
1123232812 11232328 2 SS Trastuzumab TRASTUZUMAB 1 Subcutaneous 103792 600 MG SOLUTION FOR INJECTION Q3W
1123232812 11232328 3 SS DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) 0 140 MG Q3W
1123232812 11232328 4 C CHLORPHENIRAMINE. CHLORPHENIRAMINE 1 Intravenous (not otherwise specified) 0 10 MG Q3W
1123232812 11232328 5 C ASPIRIN. ASPIRIN 1 Oral 0 75 MG TABLET QD
1123232812 11232328 6 C ATORVASTATIN ATORVASTATIN 1 Oral 0 60 MG TABLET QD
1123232812 11232328 7 C DIPYRIDAMOLE. DIPYRIDAMOLE 1 Oral 0 25 MG TABLET BID
1123232812 11232328 8 C ONDANSETRON ONDANSETRON 1 Oral 0 8 MG TABLET BID
1123232812 11232328 9 C DOMPERIDONE DOMPERIDONE 1 Oral 0 10 MG TABLET
1123232812 11232328 10 C DOMPERIDONE DOMPERIDONE 1 Oral 0 30 MG TABLET
1123232812 11232328 11 C LOPERAMIDE LOPERAMIDE 1 Oral AS REQUIRED 0 2 MG TABLET
1123232812 11232328 12 C DEXAMETHASONE. DEXAMETHASONE 1 Intravenous (not otherwise specified) 0 6.6 MG Q3W
1123232812 11232328 13 C DEXAMETHASONE. DEXAMETHASONE 1 Oral 0 8 MG TABLET
1123232812 11232328 14 C DEXAMETHASONE. DEXAMETHASONE 1 Intravenous (not otherwise specified) 0 3.3 MG Q3W
1123232812 11232328 15 C DEXAMETHASONE. DEXAMETHASONE 1 Oral 0 2 MG TABLET
1123232812 11232328 16 C Granisetron GRANISETRON 1 Intravenous (not otherwise specified) 0 1 MG 1X

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1123232812 11232328 1 HER-2 positive breast cancer
1123232812 11232328 2 HER-2 positive breast cancer
1123232812 11232328 3 HER-2 positive breast cancer
1123232812 11232328 11 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
1123232812 11232328 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
1123232812 11232328 Abdominal pain
1123232812 11232328 Blood potassium decreased
1123232812 11232328 Body temperature increased
1123232812 11232328 Constipation
1123232812 11232328 Dehydration
1123232812 11232328 Diarrhoea
1123232812 11232328 Febrile neutropenia
1123232812 11232328 Melaena
1123232812 11232328 Nausea
1123232812 11232328 Neutropenia
1123232812 11232328 Neutropenic sepsis
1123232812 11232328 Oesophagitis
1123232812 11232328 Pain
1123232812 11232328 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
1123232812 11232328 1 20150326 20150728 0
1123232812 11232328 2 20150326 20150728 0
1123232812 11232328 3 20150326 20150707 0
1123232812 11232328 4 201504 0
1123232812 11232328 5 2001 0
1123232812 11232328 6 2001 0
1123232812 11232328 7 2001 0
1123232812 11232328 8 20150326 0
1123232812 11232328 9 20150326 0
1123232812 11232328 10 201504 0
1123232812 11232328 11 201504 0
1123232812 11232328 12 201504 0
1123232812 11232328 13 20150414 20150708 0
1123232812 11232328 14 20150812 20150818 0
1123232812 11232328 15 20150815 20150828 0
1123232812 11232328 16 201504 0