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
126367191 12636719 1 I 20150106 20160809 20160809 EXP PHJP2015JP000735 NOVARTIS 0.00 A Y 0.00000 20160809 CN JP JP

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
126367191 12636719 1 PS NEORAL CYCLOSPORINE 1 Oral 100 MG, QD U 50715 100 MG CAPSULE QD
126367191 12636719 2 SS NEORAL CYCLOSPORINE 1 Oral 80 MG, QD U 50715 80 MG CAPSULE QD
126367191 12636719 3 C PREDONINE//PREDNISOLONE ACETATE 2 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126367191 12636719 1 Systemic lupus erythematosus
126367191 12636719 3 Systemic lupus erythematosus

Outcome of event

Event ID CASEID OUTC COD
126367191 12636719 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126367191 12636719 Cardiac failure
126367191 12636719 Cellulitis
126367191 12636719 Disseminated intravascular coagulation
126367191 12636719 Limb injury
126367191 12636719 Loss of consciousness
126367191 12636719 Oedema
126367191 12636719 Product use issue
126367191 12636719 Renal failure
126367191 12636719 Sepsis
126367191 12636719 Vomiting
126367191 12636719 Weight increased

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

no results found

Therapies reported

no results found