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
127237031 12723703 1 I 20160830 20160908 20160908 EXP PHEH2016US022084 NOVARTIS 59.00 YR M Y 0.00000 20160908 CN US US

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
127237031 12723703 1 PS GLEEVEC IMATINIB MESYLATE 1 Unknown U 21588
127237031 12723703 2 SS NILOTINIB NILOTINIB 1 Unknown U 0
127237031 12723703 3 SS HYPER CVAD CYCLOPHOSPHAMIDECYTARABINEDEXAMETHASONEDOXORUBICINMETHOTREXATEVINCRISTINE 1 Unknown UNK 0
127237031 12723703 4 SS HYPER CVAD CYCLOPHOSPHAMIDECYTARABINEDEXAMETHASONEDOXORUBICINMETHOTREXATEVINCRISTINE 1 Unknown UNK 0
127237031 12723703 5 SS DASATINIB DASATINIB 1 Unknown FOR 10 DAYS U 0
127237031 12723703 6 SS DASATINIB DASATINIB 1 Unknown 70 MG, UNK U 0 70 MG
127237031 12723703 7 SS PONATINIB PONATINIB 1 Unknown UNK U 0
127237031 12723703 8 SS PONATINIB PONATINIB 1 Unknown 45 MG, UNK U 0 45 MG
127237031 12723703 9 SS BOSUTINIB BOSUTINIB 1 Unknown U 0
127237031 12723703 10 SS BLINATUMOMAB BLINATUMOMAB 1 Unknown U 0
127237031 12723703 11 SS BLINATUMOMAB BLINATUMOMAB 1 Unknown 28D INFUSION U 0
127237031 12723703 12 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown 40 MG, UNK U 0 40 MG
127237031 12723703 13 C COREG CARVEDILOL 1 Unknown UNK U 0
127237031 12723703 14 C COREG CARVEDILOL 1 Unknown 30 MG, QD U 0 30 MG QD
127237031 12723703 15 C COREG CARVEDILOL 1 Unknown 45 MG, QD U 0 45 MG QD
127237031 12723703 16 C CLOFARABINE CLOFARABINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127237031 12723703 1 Acute lymphocytic leukaemia
127237031 12723703 2 Product used for unknown indication
127237031 12723703 3 Acute lymphocytic leukaemia
127237031 12723703 5 Product used for unknown indication
127237031 12723703 7 Product used for unknown indication
127237031 12723703 9 Product used for unknown indication
127237031 12723703 10 Product used for unknown indication
127237031 12723703 12 Product used for unknown indication
127237031 12723703 13 Product used for unknown indication
127237031 12723703 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127237031 12723703 HO
127237031 12723703 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127237031 12723703 Acute lymphocytic leukaemia recurrent
127237031 12723703 Arteritis
127237031 12723703 Colitis
127237031 12723703 Drug ineffective
127237031 12723703 Epiploic appendagitis
127237031 12723703 Neutropenic infection
127237031 12723703 Pancytopenia
127237031 12723703 Pleural effusion
127237031 12723703 Pulmonary toxicity
127237031 12723703 Pyrexia
127237031 12723703 Rash
127237031 12723703 Renal failure
127237031 12723703 Renal impairment
127237031 12723703 Sepsis
127237031 12723703 Subdural haematoma

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
127237031 12723703 1 200709 0
127237031 12723703 3 200603 0
127237031 12723703 4 20100105 0
127237031 12723703 7 20110411 0
127237031 12723703 10 20150223 0
127237031 12723703 11 20151229 0
127237031 12723703 13 20131031 0
127237031 12723703 14 20131207 0