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
127846211 12784621 1 I 20160318 20160413 20160927 20160927 EXP PHHO2016DE005516 SANDOZ 54.00 YR M Y 93.50000 KG 20160927 OT DE DE

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
127846211 12784621 1 PS TACROLIMUS. TACROLIMUS 1 Oral 4.5 MG, (2.5-0-2) 65461 4.5 MG
127846211 12784621 2 SS CERTICAN EVEROLIMUS 1 Oral 4.5 MG, QD (2.5-0-2) 0 4.5 MG TABLET QD
127846211 12784621 3 C PREDNISONE. PREDNISONE 1 Unknown 5 MG, UNK 0 5 MG
127846211 12784621 4 C CLEXANE ENOXAPARIN SODIUM 1 Unknown UNK U 0
127846211 12784621 5 C MARCUMAR PHENPROCOUMON 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127846211 12784621 1 Renal transplant
127846211 12784621 2 Renal transplant
127846211 12784621 3 Renal transplant
127846211 12784621 4 Shunt thrombosis
127846211 12784621 5 Shunt thrombosis

Outcome of event

Event ID CASEID OUTC COD
127846211 12784621 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127846211 12784621 Venous stenosis

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
127846211 12784621 1 20150728 0
127846211 12784621 2 20150728 0
127846211 12784621 3 20150728 0
127846211 12784621 4 20151001 20151027 0
127846211 12784621 5 20151028 20160301 0