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
90600671 9060067 1 I 20130120 0 20130207 20130207 DIR 34.00 YR F N 77.30000 KG 20130205 MD 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
90600671 9060067 1 PS ESCITALOPRAM 1 ORAL Y 201312 0 40 MG QD
90600671 9060067 3 C GEODON 1 0
90600671 9060067 5 C WELLBUTRIN GENERIC 2 0
90600671 9060067 7 C PROZAC GENERIC 2 0
90600671 9060067 9 C LAMICTAL GENERIC 2 0
90600671 9060067 11 C SPIRONOLACTONE GENERICM 2 0
90600671 9060067 13 C LUNESTA 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90600671 9060067 1 Major depression
90600671 9060067 1 Obsessive-compulsive disorder

Outcome of event

Event ID CASEID OUTC COD
90600671 9060067 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
90600671 9060067 Depression
90600671 9060067 Product substitution issue
90600671 9060067 Suicidal ideation

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

Event ID CASEID RPSR COD
90600671 9060067 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
90600671 9060067 1 20130116 20130123 0