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
127556711 12755671 1 I 2015 20160912 20160916 20160916 EXP US-PFIZER INC-2016429500 PFIZER 54.00 YR M Y 0.00000 20160916 CN 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
127556711 12755671 1 PS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 Oral 150 MG, DAILY (150MG CAPSULE EVERY DAY BY MOUTH) D 20699 150 MG PROLONGED-RELEASE CAPSULE
127556711 12755671 2 C LOTREL AMLODIPINE BESYLATEBENAZEPRIL HYDROCHLORIDE 1 5-10MG CAPSULE ONCE A DAY 0 CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127556711 12755671 1 Anxiety
127556711 12755671 2 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
127556711 12755671 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127556711 12755671 Agitation
127556711 12755671 Asthenia
127556711 12755671 Bedridden
127556711 12755671 Confusional state
127556711 12755671 Constipation
127556711 12755671 Diarrhoea
127556711 12755671 Dizziness
127556711 12755671 Drug abuser
127556711 12755671 Drug dose omission
127556711 12755671 Drug effect incomplete
127556711 12755671 Feeling abnormal
127556711 12755671 Headache
127556711 12755671 Libido decreased
127556711 12755671 Tremor

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
127556711 12755671 1 20160909 0