The Safety Rates Drug Report

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Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6024660 6841780 F 6024660-7 20081111 20081226 20081231 EXP JP-BRISTOL-MYERS SQUIBB COMPANY-14438915 BRISTOL-MYERS SQUIBB COMPANY 55 YR F Y 51 KG 20081231 MD JAPAN

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6024660 1010940263 PS ABILIFY 1 ORAL 26AUG08-08SEP08(6MG/DAY);10SEP08-06OCT08(12MG);07OCT08-(18MG/DAY)
6024660 1010940264 C SEROQUEL 1 ORAL
6024660 1010940265 C OMEPRAL 2
6024660 1010940266 C PREDNISOLONE 1
6024660 1010940267 C MAGLAX 2 TABS
6024660 1010940268 C CLARITHROMYCIN 1 TABS
6024660 1010940269 C LAMISIL 1 TABS
6024660 1010940270 C HALOPERIDOL 1
6024660 1010940271 C RISPERDAL 1 TABS
6024660 1010940272 C CHLORPROMAZINE HCL 1
6024660 1010940273 C HOKUNALIN 2 TAPE
6024660 1010940274 C AKINETON 1 TABS
6024660 1010940275 C LODOPIN 2 TABS
6024660 1010940276 C HIRNAMIN 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6024660 1010940263 SCHIZOPHRENIA

Outcome of event

Event ID OUTC COD
6024660 HO

Reactions reported

Event ID PT
6024660 RED BLOOD CELL COUNT DECREASED

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6024660 1010940263 20080826
6024660 1010940265 20050201
6024660 1010940267 20070731
6024660 1010940272 20071218
6024660 1010940276 20061226