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
125363001 12536300 1 I 20160619 20160630 20160707 20160707 EXP FR-ABBVIE-16P-056-1669557-00 ABBVIE 73.00 YR M Y 0.00000 20160707 OT FR FR

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
125363001 12536300 1 PS DEPAKOTE DIVALPROEX SODIUM 1 Oral 80-110 TABLETS Y UNKNOWN 18723
125363001 12536300 2 SS ZOPICLONE ZOPICLONE 1 Oral Y UNKNOWN 0 8 DF
125363001 12536300 3 SS LYSANXIA PRAZEPAM 1 Oral Y UNKNOWN 0 24 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125363001 12536300 1 Bipolar disorder
125363001 12536300 2 Insomnia
125363001 12536300 3 Anxiety

Outcome of event

Event ID CASEID OUTC COD
125363001 12536300 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125363001 12536300 Coma
125363001 12536300 Hyperammonaemia

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
125363001 12536300 1 20160619 20160619 0
125363001 12536300 2 20160619 20160619 0
125363001 12536300 3 20160619 20160619 0