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
123413645 12341364 5 F 2016 20160905 20160506 20160920 EXP CN-FRI-1000084488 FOREST 29.00 YR F Y 0.00000 20160920 OT DK CN

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
123413645 12341364 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 30 MG Y 160301565 20822 30 MG TABLET QD
123413645 12341364 2 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown HALF A TABLET PER DAY Y 160301565 20822

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123413645 12341364 1 Anxiety

Outcome of event

Event ID CASEID OUTC COD
123413645 12341364 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123413645 12341364 Abdominal discomfort
123413645 12341364 Chest discomfort
123413645 12341364 Depressed level of consciousness
123413645 12341364 Fear
123413645 12341364 Hypotension
123413645 12341364 Memory impairment
123413645 12341364 Panic attack
123413645 12341364 Product use issue

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
123413645 12341364 1 201511 0