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
127803551 12780355 1 I 20160421 20160916 20160926 20160926 EXP PHHO2016FR013833 NOVARTIS 70.91 YR M Y 0.00000 20160926 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
127803551 12780355 1 PS MYFORTIC MYCOPHENOLATE SODIUM 1 Unknown 1080 MG, BID U 50791 1080 MG BID
127803551 12780355 2 SS MYFORTIC MYCOPHENOLATE SODIUM 1 Unknown 720 MG, BID U 50791 720 MG BID
127803551 12780355 3 SS NEORAL CYCLOSPORINE 1 Unknown U 0
127803551 12780355 4 SS NO TREATMENT RECEIVED UNSPECIFIED INGREDIENT 1 Unknown NO TREATMENT D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127803551 12780355 1 Renal transplant
127803551 12780355 3 Renal transplant
127803551 12780355 4 Renal transplant

Outcome of event

Event ID CASEID OUTC COD
127803551 12780355 HO
127803551 12780355 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127803551 12780355 Acute pulmonary oedema
127803551 12780355 Cytomegalovirus infection
127803551 12780355 Enterococcal sepsis
127803551 12780355 Klebsiella sepsis
127803551 12780355 Pancytopenia
127803551 12780355 Staphylococcal sepsis
127803551 12780355 Subclavian vein stenosis
127803551 12780355 Thrombocytopenia

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
127803551 12780355 1 20160417 0
127803551 12780355 2 20160601 0