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
112529226 11252922 6 F 2015 20160803 20150708 20160809 EXP PHHY2015BR082170 NOVARTIS 0.00 M Y 58.00000 KG 20160809 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
112529226 11252922 1 PS EXJADE DEFERASIROX 1 Oral 1000 MG (20 MG/KG), QD 21882 20 MG/KG DISPERSIBLE TABLET QD
112529226 11252922 2 SS DEFERASIROX DEFERASIROX 1 Intramuscular 1 DF, QD 0 1 DF AMPOULE QD
112529226 11252922 3 C HYDREA HYDROXYUREA 1 Oral 2 DF, QD 0 2 DF TABLET QD
112529226 11252922 4 C CARVEDILOL. CARVEDILOL 1 Oral 1 DF, QD 0 1 DF TABLET QD
112529226 11252922 5 C ENALAPRIL ENALAPRIL 1 Oral 0.5 DF, QD 0 .5 DF TABLET QD
112529226 11252922 6 C FOLIC ACID. FOLIC ACID 1 Unknown 1 DF, TID 0 1 DF TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112529226 11252922 1 Sickle cell anaemia
112529226 11252922 2 Sickle cell anaemia
112529226 11252922 3 Sickle cell anaemia
112529226 11252922 4 Product used for unknown indication
112529226 11252922 5 Product used for unknown indication
112529226 11252922 6 Cerebral disorder

Outcome of event

Event ID CASEID OUTC COD
112529226 11252922 HO
112529226 11252922 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112529226 11252922 Cerebrovascular accident
112529226 11252922 Monoparesis
112529226 11252922 Seizure
112529226 11252922 Sickle cell anaemia with crisis

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
112529226 11252922 1 2005 0