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
115758003 11575800 3 F 20160727 20150930 20160727 EXP JP-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-066433 BRISTOL MYERS SQUIBB 4.00 DEC F Y 0.00000 20160727 OT 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
115758003 11575800 1 PS ABILIFY ARIPIPRAZOLE 1 Oral N 21436
115758003 11575800 2 SS PARACETAMOL ACETAMINOPHEN 1 Oral U 0
115758003 11575800 3 SS PAROXETINE HYDROCHLORIDE. PAROXETINE HYDROCHLORIDE 1 Oral U 0
115758003 11575800 4 SS BROTIZOLAM BROTIZOLAM 1 Oral U 0
115758003 11575800 5 C SEDES G 2 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115758003 11575800 1 Persistent depressive disorder
115758003 11575800 2 Headache
115758003 11575800 3 Persistent depressive disorder
115758003 11575800 4 Persistent depressive disorder
115758003 11575800 5 Headache

Outcome of event

Event ID CASEID OUTC COD
115758003 11575800 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115758003 11575800 Off label use
115758003 11575800 Tubulointerstitial nephritis

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

no results found

Therapies reported

no results found