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
125879651 12587965 1 I 20160715 20160725 20160725 EXP GB-CONCORDIA PHARMACEUTICALS INC.-GSH201607-003692 CONCORDIA 66.00 YR M Y 0.00000 20160725 OT GB GB

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
125879651 12587965 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown UNK, UNKNOWN FREQ. U U 21959 TABLET
125879651 12587965 2 SS ADVAGRAF TACROLIMUS 1 Unknown UNK UNK, UNKNOWN FREQ. U U 0 MODIFIED-RELEASE CAPSULE, HARD
125879651 12587965 3 SS ADVAGRAF TACROLIMUS 1 Unknown UNK UNK, UNKNOWN FREQ. U U 0 MODIFIED-RELEASE CAPSULE, HARD
125879651 12587965 4 SS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Unknown UNK UNK, UNKNOWN FREQ. U U 0 TABLET
125879651 12587965 5 SS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Unknown UNK UNK, UNKNOWN FREQ. U U 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125879651 12587965 1 Immunosuppression
125879651 12587965 2 Immunosuppression
125879651 12587965 3 Immunosuppression
125879651 12587965 4 Immunosuppression
125879651 12587965 5 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
125879651 12587965 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125879651 12587965 Renal disorder

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

no results found

Therapies reported

no results found