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
118875373 11887537 3 F 20151005 20160906 20160105 20160915 EXP PHHO2015FR019589 NOVARTIS 50.39 YR M Y 0.00000 20160915 MD FR FR

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
118875373 11887537 1 SS CERTICAN EVEROLIMUS 1 Oral 0.75 MG, BID 85.5 MG 0 .75 MG BID
118875373 11887537 2 SS CERTICAN EVEROLIMUS 1 Oral 0.75 MG, BID 85.5 MG 0 .75 MG BID
118875373 11887537 3 PS NEORAL CYCLOSPORINE 1 Unknown 75 MG, BID 50715 75 MG BID
118875373 11887537 4 C MYFORTIC MYCOPHENOLATE SODIUM 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118875373 11887537 1 Renal transplant
118875373 11887537 3 Renal transplant
118875373 11887537 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118875373 11887537 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118875373 11887537 Acute kidney injury
118875373 11887537 Lymphocele
118875373 11887537 Renal impairment

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
118875373 11887537 1 20150810 20151020 0
118875373 11887537 2 20160107 0
118875373 11887537 3 20150908 0
118875373 11887537 4 20151021 20160106 0