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
102229723 10222972 3 F 20160627 20140607 20160705 EXP PHHY2014AT069423 NOVARTIS 0.00 A M Y 106.00000 KG 20160705 OT AT AT

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
102229723 10222972 1 PS STI571 IMATINIB MESYLATE 1 Unknown 400 MG, UNK U 21588 400 MG
102229723 10222972 2 SS TASIGNA NILOTINIB 1 Unknown LESS THAN 400 MG, TWICE DAILY (BID) U 0 CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102229723 10222972 1 Chronic myeloid leukaemia
102229723 10222972 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
102229723 10222972 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
102229723 10222972 Dyspnoea
102229723 10222972 Interstitial lung disease
102229723 10222972 Lung disorder
102229723 10222972 Obesity
102229723 10222972 Pain in extremity
102229723 10222972 Polyneuropathy

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found