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
126344721 12634472 1 I 20160804 0 20160808 20160808 DIR 18.00 YR F N 165.00000 LBS 20160805 N PH 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
126344721 12634472 1 PS MYFORTIC MYCOPHENOLATE SODIUM 1 Oral N D 0 720 MG BID
126344721 12634472 3 C FENOFIBRATE. FENOFIBRATE 1 0
126344721 12634472 5 C PANTOPRAZOLE SOD PANTOPRAZOLE SODIUM 1 0
126344721 12634472 7 C RISPERIDONE. RISPERIDONE 1 0
126344721 12634472 9 C OXCARBAZEPINE. OXCARBAZEPINE 1 0
126344721 12634472 10 C MONTELUKAST MONTELUKAST SODIUM 1 0
126344721 12634472 12 C VALGANCICLOVIR. VALGANCICLOVIR 1 0
126344721 12634472 14 C MAGNESIUM OXIDE. MAGNESIUM OXIDE 1 0
126344721 12634472 16 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126344721 12634472 1 Renal transplant

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126344721 12634472 Diarrhoea

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

Event ID CASEID RPSR COD
126344721 12634472 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126344721 12634472 1 20150501 20160805 0