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
126909952 12690995 2 F 20160920 20160826 20160926 EXP PHHY2016MX116988 NOVARTIS 0.00 F Y 0.00000 20160926 MD MX MX

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
126909952 12690995 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 4.6 MG, (PATCH 5 CM2) 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM
126909952 12690995 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 9.5 MG, QD (PATCH 10 CM 2) 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126909952 12690995 3 C GABAPENTIN. GABAPENTIN 1 Unknown U 0
126909952 12690995 4 C MICARDIS TELMISARTAN 1 Unknown U 0
126909952 12690995 5 C MELOX MELOXICAM 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126909952 12690995 1 Vein disorder
126909952 12690995 3 Product used for unknown indication
126909952 12690995 4 Product used for unknown indication
126909952 12690995 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126909952 12690995 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126909952 12690995 Arthropathy
126909952 12690995 Balance disorder
126909952 12690995 Dry mouth
126909952 12690995 Dysphemia
126909952 12690995 Eye injury
126909952 12690995 Fall
126909952 12690995 Gait disturbance
126909952 12690995 Head injury
126909952 12690995 Headache
126909952 12690995 Nasal injury
126909952 12690995 Peripheral swelling
126909952 12690995 Product use issue
126909952 12690995 Thrombosis

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

no results found

Therapies reported

no results found