The Safety Rates Drug Report

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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
125089212 12508921 2 F 20160713 20160629 20160727 EXP US-APOTEX-2016AP009411 APOTEX JEONG D, DOGGETT P, SWARTZ K, HERSH L, SALZMAN B.. RECURRENT SIADH AFTER SWITCHING CITALOPRAM TO VERY LOW DOSE DULOXETINE IN THE ELDERLY.. J-AM-GERIATR-SOC 2016. 2016;64 (SUPPL. 1):S23-S24. 86.00 YR M Y 0.00000 20160727 OT 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
125089212 12508921 1 SS DULOXETINE HYDROCHLORIDE DELAYED-RELEASE CAPSULES DULOXETINE HYDROCHLORIDE 1 Unknown 20 MG, QD Y 0 20 MG CAPSULE
125089212 12508921 2 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 10 MG, QD Y 77046 10 MG TABLET
125089212 12508921 3 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 30 MG, QD Y 77046 30 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125089212 12508921 1 Depression
125089212 12508921 2 Depression

Outcome of event

Event ID CASEID OUTC COD
125089212 12508921 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125089212 12508921 Hyponatraemia
125089212 12508921 Inappropriate antidiuretic hormone secretion

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found