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
125692391 12569239 1 I 20160229 20160719 20160719 EXP PHHY2016BR029662 NOVARTIS 0.00 M Y 28.90000 KG 20160719 MD BR BR

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
125692391 12569239 1 PS EXJADE DEFERASIROX 1 Oral 25 MG/KG, QD (1 TABLET OF 500 MG AND 1 TABLET OF 250 MG) 21882 25 MG/KG DISPERSIBLE TABLET QD
125692391 12569239 2 SS EXJADE DEFERASIROX 1 Oral 25 MG/KG, QD (1 TABLET OF 500 MG AND 1 TABLET OF 250 MG) 21882 25 MG/KG DISPERSIBLE TABLET QD
125692391 12569239 3 SS EXJADE DEFERASIROX 1 Oral 500 MG, UNK 21882 500 MG DISPERSIBLE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125692391 12569239 1 Sickle cell anaemia

Outcome of event

Event ID CASEID OUTC COD
125692391 12569239 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125692391 12569239 Abdominal pain
125692391 12569239 Arthralgia
125692391 12569239 Back pain
125692391 12569239 Chest pain
125692391 12569239 Malaise
125692391 12569239 Musculoskeletal pain

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found