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
127548422 12754842 2 F 201608 20160919 20160916 20160922 EXP FR-PFIZER INC-2016428318 PFIZER 81.00 YR M Y 0.00000 20160922 OT FR FR

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
127548422 12754842 1 PS NEURONTIN GABAPENTIN 1 Oral 300 MG, 1X/DAY 20235 300 MG CAPSULE, HARD QD
127548422 12754842 2 C TAMSULOSIN TAMSULOSIN 1 0.4 MG, DAILY 0 .4 MG
127548422 12754842 3 C AVODART DUTASTERIDE 1 0.5 MG, 1X/DAY 0 .5 MG QD
127548422 12754842 4 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 1 DF, 1X/DAY 0 1 DF QD
127548422 12754842 5 C SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 1 DF, 2X/DAY 0 1 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127548422 12754842 1 Herpes zoster

Outcome of event

Event ID CASEID OUTC COD
127548422 12754842 OT
127548422 12754842 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127548422 12754842 Abnormal behaviour
127548422 12754842 Agitation
127548422 12754842 Confusional state
127548422 12754842 Eating disorder
127548422 12754842 Faecaloma
127548422 12754842 Fall
127548422 12754842 Hyponatraemia
127548422 12754842 Somnolence

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
127548422 12754842 1 20160817 20160826 0