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
89909168 8990916 8 F 20080701 20160722 20121231 20160728 EXP PHHY2012CA120973 NOVARTIS 70.67 YR F Y 0.00000 20160728 CN COUNTRY NOT SPECIFIED 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
89909168 8990916 1 PS TASIGNA NILOTINIB 1 Oral 400 MG, BID 22068 400 MG CAPSULE BID
89909168 8990916 2 SS TASIGNA NILOTINIB 1 Oral 150 MG, BID 22068 150 MG CAPSULE BID
89909168 8990916 3 C PREDNISONE. PREDNISONE 1 Unknown U 0
89909168 8990916 4 C PREDNISONE. PREDNISONE 1 U 0
89909168 8990916 5 C BABY ASPIRIN ASPIRIN 1 Unknown U 0
89909168 8990916 6 C BABY ASPIRIN ASPIRIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89909168 8990916 1 Chronic myeloid leukaemia
89909168 8990916 3 Chronic obstructive pulmonary disease
89909168 8990916 4 Lung disorder
89909168 8990916 5 Chronic obstructive pulmonary disease
89909168 8990916 6 Lung disorder

Outcome of event

Event ID CASEID OUTC COD
89909168 8990916 OT
89909168 8990916 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
89909168 8990916 Balance disorder
89909168 8990916 Dizziness
89909168 8990916 Dyspepsia
89909168 8990916 Headache
89909168 8990916 Muscular weakness
89909168 8990916 Oropharyngeal pain
89909168 8990916 Pneumonia
89909168 8990916 Speech disorder
89909168 8990916 Visual impairment

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
89909168 8990916 1 20080701 0
89909168 8990916 2 2009 0