The Safety Rates Drug Report

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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
125290771 12529077 1 I 201606 20160628 20160705 20160705 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-054400 BRISTOL MYERS SQUIBB 62.49 YR F Y 0.00000 20160705 OT 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
125290771 12529077 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 2.5 MG, QD N 21436 2.5 MG QD
125290771 12529077 2 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Oral 5 MG, QD U 0 5 MG QD
125290771 12529077 3 C PAXIL PAROXETINE HYDROCHLORIDE 1 Unknown U 0
125290771 12529077 4 C CLONAZEPAM. CLONAZEPAM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125290771 12529077 1 Depression
125290771 12529077 2 Depression
125290771 12529077 3 Product used for unknown indication
125290771 12529077 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125290771 12529077 Back injury
125290771 12529077 Dysarthria
125290771 12529077 Hyperhidrosis
125290771 12529077 Movement disorder
125290771 12529077 Rash macular
125290771 12529077 Somnolence
125290771 12529077 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
125290771 12529077 1 20160616 0
125290771 12529077 2 20160623 0