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
126695251 12669525 1 I 20160806 20160819 20160819 EXP US-CONCORDIA PHARMACEUTICALS INC.-CO-KX-US-2016-020 CONCORDIA 50.00 YR F Y 0.00000 20160819 OT 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
126695251 12669525 1 PS KAYEXALATE SODIUM POLYSTYRENE SULFONATE 1 Oral Y 0 15 MG
126695251 12669525 2 SS PREDNISONE. PREDNISONE 1 U 0
126695251 12669525 3 SS CYCLOSPORINE. CYCLOSPORINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126695251 12669525 1 Hyperkalaemia
126695251 12669525 2 Immunosuppression
126695251 12669525 3 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
126695251 12669525 HO
126695251 12669525 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126695251 12669525 Abdominal pain
126695251 12669525 Abdominal tenderness
126695251 12669525 Acute kidney injury
126695251 12669525 Gastrointestinal necrosis
126695251 12669525 Hypovolaemia
126695251 12669525 Large intestine perforation

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

no results found

Therapies reported

no results found