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
125256972 12525697 2 F 20121031 20160629 20160705 20160720 EXP DK-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-052712 BRISTOL MYERS SQUIBB 15.61 YR F Y 80.00000 KG 20160720 CN DK DK

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
125256972 12525697 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 1 DF, UNK Y 21436 1 DF
125256972 12525697 2 C SERTRALINE SERTRALINE HYDROCHLORIDE 1 Oral 75 MG, QD U 0 75 MG QD
125256972 12525697 3 C TRUXAL /00012101/ CHLORPROTHIXENE 1 Unknown 30 MG, UNK U 0 30 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125256972 12525697 1 Anxiety
125256972 12525697 2 Depression
125256972 12525697 3 Sedative therapy

Outcome of event

Event ID CASEID OUTC COD
125256972 12525697 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125256972 12525697 Apathy
125256972 12525697 Bruxism
125256972 12525697 Constipation
125256972 12525697 Derealisation
125256972 12525697 Dystonia
125256972 12525697 Eye swelling
125256972 12525697 Hiccups
125256972 12525697 Product use issue
125256972 12525697 Restlessness
125256972 12525697 Speech disorder
125256972 12525697 Strabismus
125256972 12525697 Tic
125256972 12525697 Tongue movement disturbance

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
125256972 12525697 1 20120416 0
125256972 12525697 2 20130404 20160201 0
125256972 12525697 3 20141003 20150121 0