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
1067928812 10679288 12 F 20150625 20160912 20141229 20160923 EXP CA-INCYTE CORPORATION-2013IN002396 INCYTE 80.82 YR F Y 0.00000 20160923 CN CA CA

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
1067928812 10679288 1 PS JAKAFI RUXOLITINIB 1 Oral 10 MG, BID N 202192 10 MG TABLET BID
1067928812 10679288 2 SS JAKAFI RUXOLITINIB 1 Oral 3 DF, TID N 202192 3 DF TABLET TID
1067928812 10679288 3 SS JAKAFI RUXOLITINIB 1 Oral 2 DF, BID N 202192 2 DF TABLET BID
1067928812 10679288 4 SS JAKAFI RUXOLITINIB 1 Oral 5 MG, BID N 202192 5 MG TABLET BID
1067928812 10679288 5 SS JAKAFI RUXOLITINIB 1 Oral 15 MG, QD (1 PILL OF 5 MG QAM AND 2 PILLS OF 5 MG QPM) N 202192 TABLET
1067928812 10679288 6 SS JAKAFI RUXOLITINIB 1 Oral 20 MG, QD (2 PILLS OF 5 MG IN THE MORNING AND 2 PILLS OF 5 MG IN THE EVENING) N 202192 TABLET
1067928812 10679288 7 SS JAKAFI RUXOLITINIB 1 Oral 15 MG, QD (1 PILL OF 5 MG QAM AND 2 PILLS OF 5 MG QPM) N 202192 TABLET
1067928812 10679288 8 SS JAKAFI RUXOLITINIB 1 Oral 5 MG, BID N 202192 5 MG TABLET BID
1067928812 10679288 9 SS VOLTAREN DICLOFENAC SODIUM 1 Topical UNK UNK, QD (2-3 TIMES) 0 CREAM
1067928812 10679288 10 C LIPITOR ATORVASTATIN CALCIUM 1 Unknown UNK U 0
1067928812 10679288 11 C ASA ASPIRIN 1 Unknown UNK U U 0
1067928812 10679288 12 C ASA ASPIRIN 1 Unknown 81 MG, QD U U 0 81 MG QD
1067928812 10679288 13 C ASA ASPIRIN 1 81 MG, QD U U 0 81 MG QD
1067928812 10679288 14 C CALCIUM CALCIUM 1 Unknown UNK U U 0
1067928812 10679288 15 C CALCIUM CALCIUM 1 Unknown UNK U U 0
1067928812 10679288 16 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown UNK N U 0
1067928812 10679288 17 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 20 MG, QD N U 0 20 MG QD
1067928812 10679288 18 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 10 MG, QD N U 0 10 MG QD
1067928812 10679288 19 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 20 MG, QD N U 0 20 MG QD
1067928812 10679288 20 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 10 MG, QD N U 0 10 MG QD
1067928812 10679288 21 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 20 MG, QD N U 0 20 MG QD
1067928812 10679288 22 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 10 MG, QD N U 0 10 MG QD
1067928812 10679288 23 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 20 MG, QD N U 0 20 MG QD
1067928812 10679288 24 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 10 MG, QD N U 0 10 MG QD
1067928812 10679288 25 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 20 MG, QD N U 0 20 MG QD
1067928812 10679288 26 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 10 MG, QD N U 0 10 MG QD
1067928812 10679288 27 C CELEBREX CELECOXIB 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1067928812 10679288 1 Myelofibrosis
1067928812 10679288 9 Arthritis
1067928812 10679288 10 Product used for unknown indication
1067928812 10679288 11 Product used for unknown indication
1067928812 10679288 14 Product used for unknown indication
1067928812 10679288 16 Product used for unknown indication
1067928812 10679288 27 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
1067928812 10679288 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1067928812 10679288 Abdominal distension
1067928812 10679288 Anaemia
1067928812 10679288 Arthralgia
1067928812 10679288 Contusion
1067928812 10679288 Drug ineffective
1067928812 10679288 Dry mouth
1067928812 10679288 Fatigue
1067928812 10679288 Flatulence
1067928812 10679288 Increased appetite
1067928812 10679288 Initial insomnia
1067928812 10679288 Loss of consciousness
1067928812 10679288 Muscle spasms
1067928812 10679288 Neuralgia
1067928812 10679288 Pain
1067928812 10679288 Pain in extremity
1067928812 10679288 Peripheral swelling
1067928812 10679288 Peripheral vascular disorder
1067928812 10679288 Platelet count decreased
1067928812 10679288 Pruritus
1067928812 10679288 Renal pain
1067928812 10679288 Vascular rupture
1067928812 10679288 Vomiting
1067928812 10679288 Weight increased

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
1067928812 10679288 1 20130815 0
1067928812 10679288 4 20131126 0