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
126175791 12617579 1 I 20160720 20160803 20160803 EXP US-VELOXIS PHARMACEUTICALS-1055801 VELOXIS PHARMACEUTICALS TANTISATTAMO E., CHOKECHANACHAISAKUL A., PITUKWEERAKUL S., RATANASRIMETHA P., SHRIVASTAVA P., SAMARAPUNGAVAN D. CALCINEURIN INHIBITOR-INDUCED HYPERKALEMIA AND SALTSENSITIVE HYPERTENSION IN EARLY POST-KIDNEY TRANSPLANT PERIOD. FASEB JOURNAL. 2016 65.00 YR M Y 0.00000 20160803 OT 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
126175791 12617579 1 PS ENVARSUS XR TACROLIMUS 1 U U 206406 PROLONGED-RELEASE TABLET
126175791 12617579 2 SS SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 0
126175791 12617579 3 C MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 0
126175791 12617579 4 C PREDNISONE. PREDNISONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126175791 12617579 1 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
126175791 12617579 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126175791 12617579 Hyperkalaemia
126175791 12617579 Hypertension
126175791 12617579 Metabolic acidosis
126175791 12617579 Renal tubular disorder

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

no results found

Therapies reported

no results found