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
126278161 12627816 1 I 20160725 20160806 20160806 EXP US-AUROBINDO-AUR-APL-2016-09965 AUROBINDO WILBERGER AC, ET AL.. MYCOPHENOLATE MOFETIL/PREDNISONE/ TACROLIMUS :. REACTIONS WEEKLY. 2016;1611,:129 61.00 YR M Y 0.00000 20160806 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
126278161 12627816 1 PS PREDNISONE. PREDNISONE 1 Unknown U U 84774
126278161 12627816 2 SS TACROLIMUS. TACROLIMUS 1 Unknown U U 0
126278161 12627816 3 SS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126278161 12627816 1 Immunosuppression
126278161 12627816 2 Immunosuppression
126278161 12627816 3 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
126278161 12627816 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126278161 12627816 Amnesia
126278161 12627816 Bone lesion
126278161 12627816 Confusional state
126278161 12627816 Facial paralysis
126278161 12627816 Gait disturbance
126278161 12627816 Nausea
126278161 12627816 Plasma cell myeloma
126278161 12627816 Post transplant lymphoproliferative disorder
126278161 12627816 Speech disorder
126278161 12627816 Vomiting

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

no results found

Therapies reported

no results found