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
121310103 12131010 3 F 201508 20160801 20160301 20160805 EXP PHHY2015CO153716 NOVARTIS 59.77 YR M Y 70.00000 KG 20160805 CN COUNTRY NOT SPECIFIED CO

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
121310103 12131010 1 PS TASIGNA NILOTINIB 1 Oral 150 MG, QID S0020 22068 150 MG CAPSULE QID
121310103 12131010 2 C ATORVASTATIN ATORVASTATIN 1 Unknown 20 MG, QD U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121310103 12131010 1 Chronic myeloid leukaemia
121310103 12131010 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121310103 12131010 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121310103 12131010 Asthenia
121310103 12131010 Blood pressure increased
121310103 12131010 Chest pain
121310103 12131010 Decreased appetite
121310103 12131010 Diaphragmatic disorder
121310103 12131010 Fatigue
121310103 12131010 General physical health deterioration
121310103 12131010 Incorrect drug administration duration
121310103 12131010 Pain
121310103 12131010 Pain in extremity
121310103 12131010 Splenomegaly
121310103 12131010 Tachycardia
121310103 12131010 Weight decreased
121310103 12131010 Yellow skin

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
121310103 12131010 1 20120224 0