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
126207641 12620764 1 I 201507 20160728 20160804 20160804 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-063441 BRISTOL MYERS SQUIBB 20.00 YR F Y 0.00000 20160804 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
126207641 12620764 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 5 MG, QD 21436 5 MG QD
126207641 12620764 2 SS ABILIFY ARIPIPRAZOLE 1 Oral 10 MG, QD 21436 10 MG QD
126207641 12620764 3 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126207641 12620764 1 Anxiety
126207641 12620764 2 Major depression
126207641 12620764 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126207641 12620764 Depression
126207641 12620764 Metabolic disorder
126207641 12620764 Product use issue
126207641 12620764 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
126207641 12620764 1 201507 0
126207641 12620764 2 201603 20160728 0