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
127338981 12733898 1 I 20160907 20160912 20160912 EXP FR-ROCHE-1827139 ROCHE 71.00 YR F Y 0.00000 20160912 MD FR FR

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
127338981 12733898 1 PS XELODA CAPECITABINE 1 Oral U 20896 2 DF QD
127338981 12733898 2 SS HYDREA HYDROXYUREA 1 Oral U 0 1 DF QD
127338981 12733898 3 C TEMERIT NEBIVOLOL 1 Unknown 0 5 MG
127338981 12733898 4 C TARDYFERON (FRANCE) 2 0
127338981 12733898 5 C COAPROVEL HYDROCHLOROTHIAZIDEIRBESARTAN 1 Unknown 300/25 MG 0
127338981 12733898 6 C ESOMEPRAZOLE ESOMEPRAZOLE 1 0
127338981 12733898 7 C ESBERIVEN FORT MELILOTUS OFFICINALIS TOPRUTIN 1 0
127338981 12733898 8 C TILCOTIL TENOXICAM 1 Unknown 0 20 MG
127338981 12733898 9 C KARDEGIC ASPIRIN LYSINE 1 Unknown 0 75 MG
127338981 12733898 10 C HYDREA HYDROXYUREA 1 Unknown 1 CAPSULE/DAY 0 CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127338981 12733898 1 Colorectal adenocarcinoma
127338981 12733898 2 Essential thrombocythaemia

Outcome of event

Event ID CASEID OUTC COD
127338981 12733898 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127338981 12733898 Agranulocytosis
127338981 12733898 Anaemia
127338981 12733898 Bone marrow failure
127338981 12733898 Thrombocytopenia

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
127338981 12733898 1 20160805 20160816 0
127338981 12733898 2 201512 20160816 0
127338981 12733898 10 201512 0