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
117578352 11757835 2 F 201510 20160812 20151120 20160819 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-079381 BRISTOL MYERS SQUIBB 54.08 YR M Y 175.00000 KG 20160819 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
117578352 11757835 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 2.5 MG, QD Y 21436 2.5 MG TABLET QD
117578352 11757835 2 SS ABILIFY ARIPIPRAZOLE 1 Oral 5 MG, UNK Y 21436 5 MG TABLET QD
117578352 11757835 3 C NORPRAMIN /00043102/ 2 Unknown 25 MG, UNK U 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117578352 11757835 1 Depression
117578352 11757835 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117578352 11757835 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117578352 11757835 Depression
117578352 11757835 Pain in extremity
117578352 11757835 Panic attack
117578352 11757835 Restlessness
117578352 11757835 Withdrawal syndrome
117578352 11757835 Wrong technique in product usage process

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
117578352 11757835 1 20150824 0
117578352 11757835 2 201510 0