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
121665773 12166577 3 F 20160129 20160712 20160309 20160720 EXP PHHO2016US001704 SANDOZ 22.75 YR F Y 64.10000 KG 20160720 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
121665773 12166577 1 SS CERTICAN EVEROLIMUS 1 Oral 2.25 MG, BID 0 2.25 MG TABLET BID
121665773 12166577 2 PS PREDNISONE. PREDNISONE 1 Oral 10 MG, QD 188 MG 80336 10 MG QD
121665773 12166577 3 SS PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Oral 5 MG, BID 0 5 MG BID
121665773 12166577 4 SS THYMOGLOBULIN LAPINE T-LYMPHOCYTE IMMUNE GLOBULIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121665773 12166577 1 Renal transplant
121665773 12166577 2 Renal transplant
121665773 12166577 3 Renal transplant
121665773 12166577 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121665773 12166577 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121665773 12166577 Blood creatinine increased
121665773 12166577 Groin abscess
121665773 12166577 Pneumonia
121665773 12166577 Transplant rejection

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
121665773 12166577 1 20151116 0
121665773 12166577 2 20151116 0
121665773 12166577 3 20151116 0