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
104863149 10486314 9 F 20140422 20160623 20141001 20160630 EXP PHHY2014LB051040 NOVARTIS 39.00 YR M Y 0.00000 20160630 CN COUNTRY NOT SPECIFIED LB

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
104863149 10486314 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, QD 22068 600 MG CAPSULE QD
104863149 10486314 2 C ADVIL IBUPROFEN 1 Oral UNK, PRNSOS 0
104863149 10486314 3 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 1 DF, Q12H 0 1 DF TABLET Q12H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104863149 10486314 1 Product used for unknown indication
104863149 10486314 2 Product used for unknown indication
104863149 10486314 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
104863149 10486314 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
104863149 10486314 Abdominal pain
104863149 10486314 Abdominal pain upper
104863149 10486314 Dry skin
104863149 10486314 Exposure via father
104863149 10486314 Fatigue
104863149 10486314 Gastritis
104863149 10486314 Granuloma skin
104863149 10486314 Headache
104863149 10486314 Helicobacter infection
104863149 10486314 Intentional product misuse
104863149 10486314 Leukocytosis
104863149 10486314 Neck pain
104863149 10486314 Sinusitis

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
104863149 10486314 1 20140417 0
104863149 10486314 3 201509 0