The Safety Rates Drug Report

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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
126926561 12692656 1 I 20160822 20160829 20160829 EXP US-HORIZON-PRE-0254-2016 HORIZON MURAKAMI N, BORGES TJ, YAMASHITA M, RIELLA LV. SEVERE ACUTE INTERSTITIAL NEPHRITIS AFTER COMBINATION?IMMUNE-CHECKPOINT INHIBITOR THERAPY FOR METASTATIC?MELANOMA. CKJ 2016;9(3):411-417.? 75.00 YR E M Y 0.00000 20160826 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
126926561 12692656 1 PS PREDNISONE. PREDNISONE 1 60 MG DAILY, TAPER U 202020 60 MG
126926561 12692656 2 SS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 Intravenous (not otherwise specified) 500 MG INTRAVENOUS STEROID PULSE FOR 3 DAYS, INCREASED TO 140 MG TWICE A DAY U 0 500 MG
126926561 12692656 3 SS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 1000 MG BID U 0 1000 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126926561 12692656 1 Tubulointerstitial nephritis
126926561 12692656 2 Tubulointerstitial nephritis
126926561 12692656 3 Tubulointerstitial nephritis

Outcome of event

Event ID CASEID OUTC COD
126926561 12692656 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126926561 12692656 Pseudomonas infection
126926561 12692656 Septic shock

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

no results found

Therapies reported

no results found