The Safety Rates Drug Report

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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
118140473 11814047 3 F 20140124 20160606 20151209 20160701 EXP PHHY2015TW062973 NOVARTIS 49.89 YR M Y 0.00000 20160701 MD TW TW

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
118140473 11814047 1 PS TASIGNA NILOTINIB 1 Oral 400 MG, UNK 22068 400 MG CAPSULE
118140473 11814047 2 C NORVASC AMLODIPINE BESYLATE 1 Oral 2.5 MG, UNK Y 0 2.5 MG
118140473 11814047 3 C NACID 2 Oral 1000 MG, UNK Y 0 1000 MG
118140473 11814047 4 C CB 2 Unknown 5 MG, UNK Y 0 5 MG
118140473 11814047 5 C SOLAXIN 2 Oral 200 MG, UNK U 0 200 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118140473 11814047 1 Chronic myeloid leukaemia
118140473 11814047 2 Prophylaxis
118140473 11814047 3 Prophylaxis
118140473 11814047 4 Prophylaxis
118140473 11814047 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118140473 11814047 Pruritus
118140473 11814047 Rash
118140473 11814047 Rhinorrhoea
118140473 11814047 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
118140473 11814047 1 20131018 0
118140473 11814047 2 20141208 20150105 0
118140473 11814047 3 20141208 20141222 0
118140473 11814047 4 20141208 20150105 0
118140473 11814047 5 20140124 20140207 0