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
127074672 12707467 2 F 201606 20160825 20160901 20160902 EXP PHHY2016BR118453 SANDOZ 92.02 YR F Y 63.00000 KG 20160902 CN COUNTRY NOT SPECIFIED 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
127074672 12707467 1 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 5 CM2, QD Y 0 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD
127074672 12707467 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 15 CM2, QD Y 0 13.3 MG TRANS-THERAPEUTIC-SYSTEM QD
127074672 12707467 3 PS NEOTIAPIM QUETIAPINE 1 Oral 25 MG, QD 78679 25 MG FILM-COATED TABLET QD
127074672 12707467 4 SS NEOTIAPIM QUETIAPINE 1 Oral 50 MG, QD 78679 50 MG FILM-COATED TABLET QD
127074672 12707467 5 SS DEPAKOTE DIVALPROEX SODIUM 1 Oral 0.5 DF, QD 0 .5 DF TABLET QD
127074672 12707467 6 SS DEPAKOTE DIVALPROEX SODIUM 1 Oral 1 DF, QD, BEFORE DINNER 0 1 DF TABLET QD
127074672 12707467 7 SS HEIMER MEMANTINE HYDROCHLORIDE 1 Oral UNK UNK, BID 0 TABLET BID
127074672 12707467 8 SS HEIMER MEMANTINE HYDROCHLORIDE 1 Oral UNK, QD 0 TABLET QD
127074672 12707467 9 C ALOIS MEMANTINE 1 Oral UNK UNK, BID 0 TABLET BID
127074672 12707467 10 C ALOIS MEMANTINE 1 Oral UNK, QD 0 TABLET QD
127074672 12707467 11 C QUEROPAX QUETIAPINE FUMARATE 1 Oral 25 MG, QD 0 25 MG TABLET QD
127074672 12707467 12 C QUEROPAX QUETIAPINE FUMARATE 1 Oral 0.5 DF (100 MG), QD 0 .5 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127074672 12707467 1 Dementia Alzheimer's type
127074672 12707467 5 Aggression
127074672 12707467 7 Dementia
127074672 12707467 9 Dementia
127074672 12707467 11 Sleep disorder

Outcome of event

Event ID CASEID OUTC COD
127074672 12707467 OT
127074672 12707467 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127074672 12707467 Aggression
127074672 12707467 Agitation
127074672 12707467 Asthenia
127074672 12707467 Blood pressure increased
127074672 12707467 Cerebrovascular accident
127074672 12707467 Decreased appetite
127074672 12707467 Dementia
127074672 12707467 Dizziness
127074672 12707467 Emotional disorder
127074672 12707467 Fall
127074672 12707467 Fatigue
127074672 12707467 Gait disturbance
127074672 12707467 Headache
127074672 12707467 Ischaemia
127074672 12707467 Movement disorder
127074672 12707467 Muscular weakness
127074672 12707467 Screaming
127074672 12707467 Sluggishness

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
127074672 12707467 1 200701 0
127074672 12707467 5 2009 0
127074672 12707467 7 2007 0