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
127740131 12774013 1 I 20140607 20160915 20160923 20160923 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-077416 BRISTOL MYERS SQUIBB 55.98 YR F Y 0.00000 20160923 OT FR FR

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
127740131 12774013 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 5 MG, QD Y 21436 5 MG TABLET QD
127740131 12774013 2 SS DEROXAT PAROXETINE HYDROCHLORIDE 1 Oral 60 MG, QD U 0 60 MG QD
127740131 12774013 3 SS DEROXAT PAROXETINE HYDROCHLORIDE 1 Oral 20 MG, UNK U 0 20 MG QD
127740131 12774013 4 SS NOZINAN /00038601/ LEVOMEPROMAZINE 1 Oral 25 MG, TID Y 0 25 MG TID
127740131 12774013 5 C NOVOMIX INSULIN ASPART 1 Unknown U 0
127740131 12774013 6 C LYSANXIA PRAZEPAM 1 Unknown U 0
127740131 12774013 7 C ATORVASTATIN ATORVASTATIN 1 Unknown U 0
127740131 12774013 8 C VICTOZA LIRAGLUTIDE 1 Unknown U 0
127740131 12774013 9 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown U 0
127740131 12774013 10 C NOVORAPID INSULIN ASPART 1 Unknown U 0
127740131 12774013 11 C NOCTAMIDE LORMETAZEPAM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127740131 12774013 1 Depression
127740131 12774013 2 Depression
127740131 12774013 4 Depression
127740131 12774013 5 Product used for unknown indication
127740131 12774013 6 Product used for unknown indication
127740131 12774013 7 Product used for unknown indication
127740131 12774013 8 Product used for unknown indication
127740131 12774013 9 Product used for unknown indication
127740131 12774013 10 Product used for unknown indication
127740131 12774013 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127740131 12774013 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127740131 12774013 Bradyphrenia
127740131 12774013 Confusional state
127740131 12774013 Dizziness
127740131 12774013 Headache
127740131 12774013 Hypokinesia
127740131 12774013 Product use issue

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found