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
127367751 12736775 1 I 20160706 20160715 20160912 20160912 EXP GB-TEVA-678266ACC TEVA 75.00 YR M Y 70.00000 KG 20160912 MD GB GB

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
127367751 12736775 1 PS DIAZEPAM. DIAZEPAM 1 Oral OVERDOSE: AMOUNT UNKNOWN U 70152
127367751 12736775 2 SS DIAZEPAM. DIAZEPAM 1 Oral 2 MG THREE TIMES DAILY AS REQUIRED U 70152
127367751 12736775 3 SS BRINTELLIX VORTIOXETINE HYDROBROMIDE 1 Oral 5 MG DAILY Y U 0 TABLET
127367751 12736775 4 SS BRINTELLIX VORTIOXETINE HYDROBROMIDE 1 Oral OVERDOSE: UNKNOWN NUMBER OF 5 MG TABLETS Y U 0 TABLET
127367751 12736775 5 SS ETHANOL ALCOHOL 1 Oral OVERDOSE: AMOUNT UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127367751 12736775 1 Product used for unknown indication
127367751 12736775 2 Anxiety
127367751 12736775 3 Depression
127367751 12736775 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127367751 12736775 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127367751 12736775 Intentional overdose
127367751 12736775 Suicide attempt

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
127367751 12736775 1 20160706 20160707 0
127367751 12736775 3 20160627 20160705 0
127367751 12736775 4 20160706 20160706 0
127367751 12736775 5 20160706 20160706 0