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
125221262 12522126 2 F 20160322 20160902 20160701 20160906 EXP JP-OTSUKA-2016_006835 OTSUKA 94.00 YR F Y 0.00000 20160906 PH JP JP

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
125221262 12522126 1 PS Pletaal OD tablets 50mg CILOSTAZOL 1 Oral 200 MG, DAILY DOSE 20863 200 MG ORODISPERSIBLE TABLET
125221262 12522126 2 SS SEROQUEL QUETIAPINE FUMARATE 1 Unknown UNK U 0 FILM-COATED TABLET
125221262 12522126 3 SS ROZEREM RAMELTEON 1 Oral UNK Y 0 FILM-COATED TABLET
125221262 12522126 4 SS FOLIAMIN FOLIC ACID 1 Oral UNK Y 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125221262 12522126 1 Product used for unknown indication
125221262 12522126 2 Product used for unknown indication
125221262 12522126 3 Product used for unknown indication
125221262 12522126 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125221262 12522126 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125221262 12522126 Blood alkaline phosphatase increased

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
125221262 12522126 2 20160116 0
125221262 12522126 3 20160116 20160324 0
125221262 12522126 4 20160116 20160324 0