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
127482161 12748216 1 I 20000626 20010320 20160915 20160915 EXP US-OTSUKA-02100-USA-01-0037 OTSUKA 76.61 YR M Y 0.00000 20160915 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
127482161 12748216 1 PS PLETAL CILOSTAZOL 1 Oral 100 MG, QD 1200 MG Y 20863 100 MG TABLET QD
127482161 12748216 2 SS PLETAL CILOSTAZOL 1 Oral 100 MG, QD 1200 MG Y 20863 100 MG TABLET QD
127482161 12748216 3 C ASPIRIN. ASPIRIN 1 Oral UNK 0
127482161 12748216 4 C CARDURA DOXAZOSIN MESYLATE 1 Oral UNK 0
127482161 12748216 5 C PRINIVIL LISINOPRIL 1 Oral UNK 0
127482161 12748216 6 C LOCOL FLUVASTATIN SODIUM 1 Oral UNK 0 TABLET
127482161 12748216 7 C ALLOPURINOL. ALLOPURINOL 1 Oral UNK 0
127482161 12748216 8 C LIPITOR ATORVASTATIN CALCIUM 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127482161 12748216 1 Intermittent claudication
127482161 12748216 3 Cardiovascular event prophylaxis
127482161 12748216 4 Hypertension
127482161 12748216 5 Hypertension
127482161 12748216 6 Diuretic therapy
127482161 12748216 7 Gout
127482161 12748216 8 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
127482161 12748216 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127482161 12748216 Myelodysplastic syndrome

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
127482161 12748216 1 20000531 20000604 0
127482161 12748216 2 20000612 20000618 0