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
107686144 10768614 4 F 20150126 20160705 20150206 20160715 EXP JP-ROCHE-1534077 ROCHE DOI Y, INOUE Y, DOI Y, ARISATO T, ET AL. A CASE OF HAEMODIALYSIS PATIENT WHO EXPERIENCED DISTURBED CONSCIOUSNESS INDUCED BY CEFTRIAXONE THERAPY.. PROCEEDINGS OF THE 61ST ANNUAL MEETING OF THE JAPANESE SOCIETY FOR DIALYSIS THERAPY; 10-12 JUN 2016, OSAKA-CITY, OSAKA; MAY 2016. 49(S1)926. 2016 MAY;49(S1):926-. 72.93 YR M Y 59.00000 KG 20160715 MD 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
107686144 10768614 1 PS ROCEPHIN CEFTRIAXONE SODIUM 1 Intravenous drip U 63239 3 G QD
107686144 10768614 2 SS ROCEPHIN CEFTRIAXONE SODIUM 1 Intravenous drip U 63239 2 G BID
107686144 10768614 3 SS ROCEPHIN CEFTRIAXONE SODIUM 1 Intravenous drip U 63239 2 G QD
107686144 10768614 4 C SPIRONOLACTONE. SPIRONOLACTONE 1 Oral 0 25 MG QD
107686144 10768614 5 C CRESTOR ROSUVASTATIN CALCIUM 1 Oral 0 7.5 MG QD
107686144 10768614 6 C BAYASPIRIN ASPIRIN 1 Oral 0 100 MG QD
107686144 10768614 7 C FAMOTIDINE. FAMOTIDINE 1 Oral 0 20 MG QD
107686144 10768614 8 C PLETAAL CILOSTAZOL 1 Oral 0 100 MG BID
107686144 10768614 9 C FOSRENOL LANTHANUM CARBONATE 1 Oral 0 250 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107686144 10768614 1 Pneumonia bacterial
107686144 10768614 2 Pneumonia bacterial
107686144 10768614 3 Pneumonia bacterial
107686144 10768614 4 Hypertension
107686144 10768614 5 Hyperlipidaemia
107686144 10768614 6 Myocardial infarction
107686144 10768614 7 Gastric ulcer
107686144 10768614 8 Cerebral infarction
107686144 10768614 9 Hyperphosphataemia

Outcome of event

Event ID CASEID OUTC COD
107686144 10768614 HO
107686144 10768614 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107686144 10768614 Altered state of consciousness
107686144 10768614 Chest discomfort
107686144 10768614 Delirium
107686144 10768614 Encephalopathy
107686144 10768614 Myoclonus
107686144 10768614 Vomiting

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
107686144 10768614 1 20150119 20150119 0
107686144 10768614 2 20150120 20150125 0
107686144 10768614 3 20150126 20150128 0