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
123178783 12317878 3 F 20160203 20160721 20160429 20160804 EXP DE-BFARM-16105004 DE-FRI-1000084130 FOREST 1.00 DY F Y 4.10000 KG 20160804 OT DK DE

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
123178783 12317878 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Transplacental 40 MG U 20822 40 MG
123178783 12317878 2 SS AMPICILLIN AMPICILLIN 1 Transplacental 0
123178783 12317878 3 SS FLUOMIZIN DEQUALINIUM CHLORIDE 1 Transplacental 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123178783 12317878 1 Obsessive-compulsive disorder
123178783 12317878 2 Urinary tract infection
123178783 12317878 3 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
123178783 12317878 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
123178783 12317878 Foetal exposure during pregnancy
123178783 12317878 Ventricular septal defect

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
123178783 12317878 1 20160203 0