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
127754942 12775494 2 F 20160921 20160923 20160929 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-077024 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160929 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
127754942 12775494 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown 30 MG, QD U 21436 30 MG QD
127754942 12775494 2 SS ABILIFY ARIPIPRAZOLE 1 U 21436
127754942 12775494 3 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Unknown 30 MG, UNK U 21436 30 MG
127754942 12775494 4 C RISPERDAL RISPERIDONE 1 Unknown U 0
127754942 12775494 5 C NORVASC AMLODIPINE BESYLATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127754942 12775494 1 Schizophrenia
127754942 12775494 2 Bipolar disorder
127754942 12775494 3 Bipolar disorder
127754942 12775494 4 Product used for unknown indication
127754942 12775494 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127754942 12775494 OT
127754942 12775494 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127754942 12775494 Blood sodium decreased
127754942 12775494 Delusion
127754942 12775494 Drug ineffective
127754942 12775494 Hallucination
127754942 12775494 Off label use

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
127754942 12775494 1 2006 0