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
109617977 10961797 7 F 201502 20160720 20150327 20160726 EXP PHHY2015PL032092 NOVARTIS 64.87 YR F Y 69.00000 KG 20160726 CN COUNTRY NOT SPECIFIED PL

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
109617977 10961797 1 PS TASIGNA NILOTINIB 1 Oral 400 MG, BID 22068 400 MG CAPSULE BID
109617977 10961797 2 C LETROX LEVOTHYROXINE SODIUM 1 Oral 100 MG (MONDAY TO FRIDAY) AND 75 MG (SATURDAY - SUNDAY) 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109617977 10961797 1 Chronic myeloid leukaemia
109617977 10961797 2 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
109617977 10961797 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
109617977 10961797 Arthralgia
109617977 10961797 Arthritis
109617977 10961797 Body temperature increased
109617977 10961797 Burning sensation
109617977 10961797 Neck pain
109617977 10961797 Peripheral swelling

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
109617977 10961797 1 201104 0
109617977 10961797 2 201104 0