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
126022021 12602202 1 I 20160726 0 20160727 20160727 DIR 69.48 YR F N 0.00000 20160726 N OT 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
126022021 12602202 1 PS MYFORTIC MYCOPHENOLATE SODIUM 1 Oral D D 0 180 MG BID
126022021 12602202 2 SS TACROLIMUS CAP 5MG TACROLIMUS 1 Oral D D 0 5 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126022021 12602202 1 Renal transplant
126022021 12602202 2 Renal transplant

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126022021 12602202 Back pain
126022021 12602202 Diarrhoea
126022021 12602202 Dizziness
126022021 12602202 Internal haemorrhage
126022021 12602202 Malaise
126022021 12602202 Micturition urgency
126022021 12602202 Nausea
126022021 12602202 Therapy cessation

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

Event ID CASEID RPSR COD
126022021 12602202 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126022021 12602202 1 20160530 0
126022021 12602202 2 20160530 0