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
127062851 12706285 1 I 20160831 20160901 20160901 EXP CA-ROCHE-1823744 ROCHE REPORTER KNOWN TO HEALTH AUTHORITY U, UNKNOWN UNKNOWN. UNKNOWN ;:-. 40.00 YR M Y 0.00000 20160901 OT CA CA

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
127062851 12706285 1 PS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Unknown U 50722
127062851 12706285 2 SS TACROLIMUS. TACROLIMUS 1 Unknown U 0 CAPSULE
127062851 12706285 3 SS TACROLIMUS. TACROLIMUS 1 Unknown U 0
127062851 12706285 4 C PREDNISONE. PREDNISONE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127062851 12706285 1 Prophylaxis against transplant rejection
127062851 12706285 2 Prophylaxis against transplant rejection
127062851 12706285 4 Prophylaxis against transplant rejection

Outcome of event

Event ID CASEID OUTC COD
127062851 12706285 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127062851 12706285 Acute kidney injury
127062851 12706285 Toxicity to various agents

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

no results found

Therapies reported

no results found