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
125795261 12579526 1 I 20160305 20160322 20160721 20160721 EXP JP-ASTRAZENECA-2016SE46630 ASTRAZENECA 94.00 YR F Y 0.00000 20160721 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
125795261 12579526 1 PS SEROQUEL QUETIAPINE FUMARATE 1 Oral 2500 MG 20639 50 MG TABLET QD
125795261 12579526 2 SS FOLIAMIN FOLIC ACID 1 Oral 0
125795261 12579526 3 SS ROZEREM RAMELTEON 1 Oral 400 MG 0 8 MG TABLET QD
125795261 12579526 4 SS PLETAAL CILOSTAZOL 1 Oral 0 200 MG QD
125795261 12579526 5 C GASTER FAMOTIDINE 1 0
125795261 12579526 6 C ENSURE AMINO ACIDSDEXTROSEELECTROLYTES NOSSOYBEAN OILVITAMINS 1 0
125795261 12579526 7 C EBASTEL EBASTINE 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125795261 12579526 1 Product used for unknown indication
125795261 12579526 2 Product used for unknown indication
125795261 12579526 3 Product used for unknown indication
125795261 12579526 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125795261 12579526 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125795261 12579526 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
125795261 12579526 1 20160116 0
125795261 12579526 3 20160116 0