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
126646321 12664632 1 I 20160811 20160818 20160818 EXP PHHY2016BR112306 NOVARTIS 0.00 F Y 80.00000 KG 20160818 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
126646321 12664632 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal (PATCH 5CM2) U 667130 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM
126646321 12664632 2 C NORIPURUM IRON POLYMALTOSE 1 Unknown U 0
126646321 12664632 3 C INSULIN INSULIN NOS 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126646321 12664632 1 Memory impairment
126646321 12664632 2 Product used for unknown indication
126646321 12664632 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126646321 12664632 HO
126646321 12664632 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126646321 12664632 Abnormal behaviour
126646321 12664632 Anaemia
126646321 12664632 Dementia
126646321 12664632 Drug-induced liver injury
126646321 12664632 Eating disorder
126646321 12664632 Emotional disorder
126646321 12664632 Nervousness
126646321 12664632 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
126646321 12664632 1 201503 0