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
125433081 12543308 1 I 20160624 20160711 20160711 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-056392 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160711 CN US 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
125433081 12543308 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown N 21436 TABLET
125433081 12543308 2 SS ARIPIPRAZOLE TEVA ARIPIPRAZOLE 1 Oral 5 MG, QD U TV7569 0 5 MG QD
125433081 12543308 3 C LIPITOR ATORVASTATIN CALCIUM 1 Unknown U 0
125433081 12543308 4 C ASPIRIN /00002701/ ASPIRIN 1 Unknown U 0
125433081 12543308 5 C CHLORTHALIDONE. CHLORTHALIDONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125433081 12543308 1 Anxiety
125433081 12543308 2 Anxiety
125433081 12543308 3 Product used for unknown indication
125433081 12543308 4 Product used for unknown indication
125433081 12543308 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125433081 12543308 Blood glucose increased
125433081 12543308 Glucose tolerance impaired
125433081 12543308 Hypertension
125433081 12543308 Product use issue
125433081 12543308 Weight increased

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
125433081 12543308 2 20160527 0