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
125937931 12593793 1 I 20140708 20160718 20160726 20160726 EXP FR-PFIZER INC-2016349243 PFIZER 84.00 YR F Y 0.00000 20160726 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
125937931 12593793 1 PS ZITHROMAX AZITHROMYCIN DIHYDRATE 1 Oral 1 DF, 3X/WEEK Y 50711 1 DF FILM-COATED TABLET
125937931 12593793 2 SS SEROPLEX ESCITALOPRAM OXALATE 1 Oral 5 MG, 1X/DAY Y 0 5 MG FILM-COATED TABLET QD
125937931 12593793 3 SS TENSTATEN CICLETANINE HYDROCHLORIDE 1 Oral 50 MG, 1X/DAY Y 0 50 MG CAPSULE QD
125937931 12593793 4 C KARDEGIC ASPIRIN LYSINE 1 UNK 0
125937931 12593793 5 C TEMERIT NEBIVOLOL 1 UNK 0
125937931 12593793 6 C FENOFIBRATE. FENOFIBRATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125937931 12593793 1 Bronchiectasis
125937931 12593793 2 Depression
125937931 12593793 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125937931 12593793 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125937931 12593793 Fall
125937931 12593793 Hyponatraemia
125937931 12593793 Vertigo

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
125937931 12593793 1 20140708 0
125937931 12593793 2 20140708 0
125937931 12593793 3 20140708 0