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
126797621 12679762 1 I 20160818 20160824 20160824 EXP PHHY2016BR114795 NOVARTIS 0.00 F Y 0.00000 20160824 CN 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
126797621 12679762 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 13.3 MG, QD (PATCH: 27 MG/ 15 CM2) U 22083 13.3 MG TRANS-THERAPEUTIC-SYSTEM QD
126797621 12679762 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 2 DF, (PATCH: 27 MG/ 15 CM2) U 22083 2 DF TRANS-THERAPEUTIC-SYSTEM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126797621 12679762 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126797621 12679762 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126797621 12679762 Abnormal faeces
126797621 12679762 Asthenia
126797621 12679762 Drug administration error
126797621 12679762 Gastrointestinal infection
126797621 12679762 Incorrect drug administration duration
126797621 12679762 Malaise
126797621 12679762 Seizure
126797621 12679762 Syncope
126797621 12679762 Vomiting

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

no results found

Therapies reported

no results found