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
126646451 12664645 1 I 20160812 20160818 20160818 EXP PHHY2016BR112356 NOVARTIS 0.00 F Y 50.00000 KG 20160818 OT 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
126646451 12664645 1 PS EXELON RIVASTIGMINE TARTRATE 1 Oral 1.5 MG, UNK 20823 1.5 MG CAPSULE
126646451 12664645 2 SS EXELON RIVASTIGMINE TARTRATE 1 Oral 3 MG, UNK 20823 3 MG CAPSULE
126646451 12664645 3 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 5 CM2 0 4.6 MG TRANS-THERAPEUTIC-SYSTEM
126646451 12664645 4 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10 CM2, QD 674210 0 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126646451 12664645 5 C AZOPT BRINZOLAMIDE 1 Ophthalmic UNK 0 SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126646451 12664645 1 Dementia Alzheimer's type
126646451 12664645 3 Dementia Alzheimer's type
126646451 12664645 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126646451 12664645 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126646451 12664645 Aspiration bronchial
126646451 12664645 Dysphagia
126646451 12664645 Mobility decreased
126646451 12664645 Pneumonia
126646451 12664645 Thrombosis
126646451 12664645 Urinary tract infection

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
126646451 12664645 4 2009 0