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
126627481 12662748 1 I 20160526 20160818 20160818 EXP US-STRIDES ARCOLAB LIMITED-2016SP004416 STRIDES 0.00 Y 0.00000 20160818 MD 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
126627481 12662748 1 PS TACROLIMUS. TACROLIMUS 1 UNK 90687
126627481 12662748 2 C MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 UNK 0
126627481 12662748 3 C PREDNISONE. PREDNISONE 1 UNK 0
126627481 12662748 4 C CYCLOSPORINE. CYCLOSPORINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126627481 12662748 1 Immunosuppression
126627481 12662748 2 Immunosuppression
126627481 12662748 3 Immunosuppression
126627481 12662748 4 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
126627481 12662748 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126627481 12662748 Ataxia
126627481 12662748 Diplopia
126627481 12662748 Dysmetria
126627481 12662748 Encephalitis brain stem
126627481 12662748 Gait disturbance
126627481 12662748 Headache
126627481 12662748 Neurotoxicity
126627481 12662748 Nystagmus

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

no results found

Therapies reported

no results found