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
126012231 12601223 1 I 20160411 20160502 20160728 20160728 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-061445 BRISTOL MYERS SQUIBB 58.07 YR F Y 70.00000 KG 20160728 CN 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
126012231 12601223 1 PS ABILIFY ARIPIPRAZOLE 1 Oral U 21436 TABLET
126012231 12601223 2 SS XEROQUEL QUETIAPINE FUMARATE 1 Oral 300 MG, UNK U 0 300 MG
126012231 12601223 3 SS ZOPICLONE ZOPICLONE 1 Oral UNK, QD U 0 7.5 MG
126012231 12601223 4 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown 60 MG, UNK U 0 60 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126012231 12601223 1 Bipolar I disorder
126012231 12601223 2 Bipolar I disorder
126012231 12601223 3 Insomnia
126012231 12601223 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126012231 12601223 HO
126012231 12601223 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126012231 12601223 Coma
126012231 12601223 Pneumonia aspiration
126012231 12601223 Product use issue
126012231 12601223 Rhabdomyolysis
126012231 12601223 Toxicity to various agents

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

no results found

Therapies reported

no results found