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
126486171 12648617 1 I 20160805 20160812 20160812 EXP PHHY2016FR108991 SANDOZ 62.00 YR F Y 0.00000 20160812 OT FR FR

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
126486171 12648617 1 PS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Unknown 65379
126486171 12648617 2 SS PREDNISONE. PREDNISONE 1 Unknown 0
126486171 12648617 3 SS TACROLIMUS. TACROLIMUS 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126486171 12648617 1 Liver transplant
126486171 12648617 2 Liver transplant
126486171 12648617 3 Liver transplant

Outcome of event

Event ID CASEID OUTC COD
126486171 12648617 DE
126486171 12648617 HO
126486171 12648617 LT
126486171 12648617 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126486171 12648617 Acute respiratory distress syndrome
126486171 12648617 Cardiorenal syndrome
126486171 12648617 Hypovolaemia
126486171 12648617 Inflammation
126486171 12648617 Lung disorder
126486171 12648617 Multiple organ dysfunction syndrome
126486171 12648617 Pulmonary oedema
126486171 12648617 Systemic inflammatory response syndrome
126486171 12648617 Toxoplasmosis

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

no results found

Therapies reported

no results found