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
89000218 8900021 8 F 2009 20160822 20121109 20160826 EXP PHHY2012BR102176 NOVARTIS 0.00 F Y 65.00000 KG 20160826 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
89000218 8900021 1 PS EXJADE DEFERASIROX 1 Oral 3 DF, QD Y 21882 3 DF DISPERSIBLE TABLET QD
89000218 8900021 2 SS EXJADE DEFERASIROX 1 Oral 1 DF, UNK Y 21882 1 DF DISPERSIBLE TABLET
89000218 8900021 3 SS EXJADE DEFERASIROX 1 Oral 2 DF, QD Y 21882 2 DF DISPERSIBLE TABLET QD
89000218 8900021 4 SS EXJADE DEFERASIROX 1 Oral 3 DF, QD Y SA055 21882 3 DF DISPERSIBLE TABLET QD
89000218 8900021 5 C ENDOFOLIN FOLIC ACID 1 Oral 2 DF, DAILY 0 2 DF QD
89000218 8900021 6 C ATENOLOL. ATENOLOL 1 Oral 2 DF, DAILY 0 2 DF QD
89000218 8900021 7 C HYDREA HYDROXYUREA 1 Oral 1 DF, QD 0 1 DF TABLET QD
89000218 8900021 8 C FOLIC ACID. FOLIC ACID 1 Unknown UNK 0
89000218 8900021 9 C CLORANA HYDROCHLOROTHIAZIDE 1 Oral 2 DF, DAILY 0 2 DF
89000218 8900021 10 C ATENOLOL W/NIFEDIPINE 2 Unknown UNK 0
89000218 8900021 11 C AAS ASPIRIN 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89000218 8900021 1 Sickle cell anaemia
89000218 8900021 5 Product used for unknown indication
89000218 8900021 6 Product used for unknown indication
89000218 8900021 7 Sickle cell anaemia
89000218 8900021 8 Product used for unknown indication
89000218 8900021 9 Product used for unknown indication
89000218 8900021 10 Product used for unknown indication
89000218 8900021 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
89000218 8900021 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
89000218 8900021 Asthenia
89000218 8900021 Blood iron increased
89000218 8900021 Diarrhoea
89000218 8900021 Dysgeusia
89000218 8900021 Dysphagia
89000218 8900021 Hypertension
89000218 8900021 Limb discomfort
89000218 8900021 Liver disorder
89000218 8900021 Malaise
89000218 8900021 Musculoskeletal discomfort
89000218 8900021 Nail discolouration
89000218 8900021 Nephrolithiasis
89000218 8900021 Osteonecrosis
89000218 8900021 Pyrexia
89000218 8900021 Renal disorder
89000218 8900021 Skin discolouration
89000218 8900021 Syncope
89000218 8900021 Vomiting
89000218 8900021 Weight increased

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
89000218 8900021 1 2005 0
89000218 8900021 2 201112 201208 0
89000218 8900021 5 19920101 0
89000218 8900021 6 20111212 0
89000218 8900021 7 2005 0
89000218 8900021 8 1992 0
89000218 8900021 9 2002 0
89000218 8900021 11 2012 0