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
126014001 12601400 1 I 20160713 20160728 20160728 EXP US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-120765 RANBAXY 61.00 YR M Y 0.00000 20160728 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
126014001 12601400 1 PS PREDNISONE. PREDNISONE 1 Unknown UNK U U 89247
126014001 12601400 2 SS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Unknown U U UNK 0
126014001 12601400 3 SS TACROLIMUS. TACROLIMUS 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126014001 12601400 1 Immunosuppression
126014001 12601400 2 Immunosuppression
126014001 12601400 3 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
126014001 12601400 DE
126014001 12601400 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126014001 12601400 Epstein-Barr viraemia
126014001 12601400 Plasma cell myeloma
126014001 12601400 Post transplant lymphoproliferative disorder
126014001 12601400 Staphylococcal infection

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

no results found

Therapies reported

no results found