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
115874334 11587433 4 F 20150812 20160803 20151001 20160810 EXP PHHY2015CR117093 NOVARTIS 0.00 DY M Y 1.71000 KG 20160810 CN COUNTRY NOT SPECIFIED CR

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
115874334 11587433 1 PS TASIGNA NILOTINIB 1 Transplacental 200 MG, BID 22068 200 MG CAPSULE BID
115874334 11587433 2 C DEXAMETASON//DEXAMETHASONE 2 Transplacental 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115874334 11587433 1 Foetal exposure during pregnancy
115874334 11587433 2 Foetal exposure during pregnancy

Outcome of event

Event ID CASEID OUTC COD
115874334 11587433 OT
115874334 11587433 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
115874334 11587433 Abdominal pain
115874334 11587433 Anaemia
115874334 11587433 Bronchiolitis
115874334 11587433 Cough
115874334 11587433 Dyspnoea
115874334 11587433 Foetal exposure during pregnancy
115874334 11587433 Immature respiratory system
115874334 11587433 Jaundice
115874334 11587433 Nasopharyngitis
115874334 11587433 Premature baby
115874334 11587433 Rhinitis
115874334 11587433 Selective eating disorder

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
115874334 11587433 2 20110811 0