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
126968521 12696852 1 I 20160817 20160830 20160830 EXP US-DRREDDYS-USA/USA/16/0082769 DR REDDYS PATEL S, KUTEN S, MUSICK W, GABER A, MONSOUR H, KNIGHT R. COMBINATION DRUG PRODUCTS FOR HIV-A WORD OF CAUTION FOR THE TRANSPLANT CLINICIAN. AM J TRANSPLANT. 2016;16(8):2479-82. 38.00 YR M Y 0.00000 20160830 PH COUNTRY NOT SPECIFIED 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
126968521 12696852 1 PS TACROLIMUS. TACROLIMUS 1 Unknown STABLE DOSE Y UNKNOWN 90509 3 MG Q12H
126968521 12696852 2 SS PREDNISONE. PREDNISONE 1 Unknown 0 7.5 MG QD
126968521 12696852 3 SS mycophenolate sodium MYCOPHENOLATE SODIUM 1 Unknown 0 360 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126968521 12696852 1 Immunosuppression
126968521 12696852 2 Immunosuppression
126968521 12696852 3 Immunosuppression

Outcome of event

Event ID CASEID OUTC COD
126968521 12696852 HO
126968521 12696852 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126968521 12696852 Acute kidney injury
126968521 12696852 Diabetes mellitus inadequate control
126968521 12696852 Diarrhoea
126968521 12696852 Drug interaction
126968521 12696852 Headache
126968521 12696852 Immunosuppressant drug level increased
126968521 12696852 Nausea
126968521 12696852 Nephropathy toxic
126968521 12696852 Visual impairment
126968521 12696852 Vomiting

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

no results found

Therapies reported

no results found