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
125622903 12562290 3 F 20160817 20160715 20160822 EXP PHEH2016US017504 NOVARTIS 0.00 F Y 0.00000 20160822 MD US US

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
125622903 12562290 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal EXELON 10 CM2 PATCH U 4405A 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
125622903 12562290 2 C COD LIVER OIL COD LIVER OIL 1 Unknown UNK U 0
125622903 12562290 3 C COCONUT OIL COCONUT OIL 1 Unknown UNK U 0
125622903 12562290 4 C VITAMIN C ASCORBIC ACID 1 Unknown UNK U 0
125622903 12562290 5 C GINKGO BILOBA GINKGO 1 Unknown UNK U 0
125622903 12562290 6 C FENOFIBRATE. FENOFIBRATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125622903 12562290 1 Product used for unknown indication
125622903 12562290 2 Product used for unknown indication
125622903 12562290 3 Product used for unknown indication
125622903 12562290 4 Product used for unknown indication
125622903 12562290 5 Product used for unknown indication
125622903 12562290 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125622903 12562290 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125622903 12562290 Hand fracture
125622903 12562290 Product adhesion issue

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

no results found

Therapies reported

no results found