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
122725182 12272518 2 F 201602 20160915 20160415 20160922 EXP PHHY2016DE049798 NOVARTIS 0.00 A M Y 0.00000 20160922 MD DE DE

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
122725182 12272518 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, QD U 22068 600 MG CAPSULE QD
122725182 12272518 2 C FOSTER//PIROXICAM 2 Unknown 4 PUFFS, UNK 0 4 DF
122725182 12272518 3 C SALBUTAMOL ALBUTEROL 1 Unknown 2 PUFFS, UNK 0 2 DF
122725182 12272518 4 C LAIF 2 Unknown 3X4050 MG, TID Y 0 4050 MG TID
122725182 12272518 5 C OMEP OMEPRAZOLE 1 Unknown 20 MG, UNK 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122725182 12272518 1 Chronic myeloid leukaemia
122725182 12272518 2 Product used for unknown indication
122725182 12272518 3 Product used for unknown indication
122725182 12272518 4 Product used for unknown indication
122725182 12272518 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122725182 12272518 Arthralgia
122725182 12272518 Dyspepsia
122725182 12272518 Rash

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
122725182 12272518 1 20151203 0
122725182 12272518 2 2014 0
122725182 12272518 3 1984 0
122725182 12272518 4 2012 20151203 0
122725182 12272518 5 20160223 0