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
126698201 12669820 1 I 201607 20160810 20160819 20160819 EXP US-PFIZER INC-2016383379 PFIZER 50.00 YR M Y 0.00000 20160819 CN 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
126698201 12669820 1 PS RAPAMUNE SIROLIMUS 1 Oral 1MG TABLET TAKE 3 TABLETS EVERY MORNING 21110 3 MG TABLET
126698201 12669820 2 C AMLODIPINE BESILATE AMLODIPINE BESYLATE 1 10 MG, 1X/DAY 0 10 MG QD
126698201 12669820 3 C PREDNISONE. PREDNISONE 1 5 MG, 1X/DAY 0 5 MG QD
126698201 12669820 4 C CLONIDINE HCL CLONIDINE HYDROCHLORIDE 1 0.1 MG, 1X/DAY 0 .1 MG QD
126698201 12669820 5 C HYDRALAZINE HCL HYDRALAZINE HYDROCHLORIDE 1 100 MG, 1X/DAY 0 100 MG QD
126698201 12669820 6 C AZATHIOPRINE. AZATHIOPRINE 1 50MG TABLE ONCE A DAY 0 50 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126698201 12669820 1 Renal transplant

Outcome of event

Event ID CASEID OUTC COD
126698201 12669820 HO
126698201 12669820 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126698201 12669820 Blood creatinine increased
126698201 12669820 Renal failure
126698201 12669820 Treatment noncompliance

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

no results found

Therapies reported

no results found