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
125594302 12559430 2 F 20160706 20160802 20160715 20160808 EXP JP-009507513-1607JPN006113 MERCK 67.00 YR M Y 67.00000 KG 20160808 PH JP JP

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
125594302 12559430 1 PS REMERON MIRTAZAPINE 1 Oral 30 MG, HS 20415 30 MG TABLET QD
125594302 12559430 2 SS REMERON MIRTAZAPINE 1 Oral 15 MG, UNK 20415 15 MG TABLET
125594302 12559430 3 C MYSLEE ZOLPIDEM TARTRATE 1 Oral 10 MG, HS U 0 10 MG TABLET QD
125594302 12559430 4 C DOGMATYL SULPIRIDE 1 Oral 50 MG, HS U 0 50 MG TABLET QD
125594302 12559430 5 C RIZE CLOTIAZEPAM 1 Oral 5 MG, QD U 0 5 MG TABLET QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125594302 12559430 OT
125594302 12559430 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125594302 12559430 Apathy
125594302 12559430 Hyponatraemia
125594302 12559430 Inappropriate antidiuretic hormone secretion
125594302 12559430 Weight decreased

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
125594302 12559430 1 20160705 0
125594302 12559430 2 20160706 0