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
115782223 11578222 3 F 20150428 20160727 20150930 20160728 EXP PHHY2015FR116292 NOVARTIS 59.00 YR F Y 55.00000 KG 20160728 MD 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
115782223 11578222 1 PS MYFORTIC MYCOPHENOLATE SODIUM 1 Oral 1440 MG, QD Y U 50791 1440 MG QD
115782223 11578222 2 SS NO TREATMENT RECEIVED UNSPECIFIED INGREDIENT 1 Unknown UNK U 0
115782223 11578222 3 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Unknown 3 MG, UNK U 0 3 MG
115782223 11578222 4 C SERESTA OXAZEPAM 1 Unknown 10 MG, UNK U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115782223 11578222 1 Liver transplant
115782223 11578222 2 Product used for unknown indication
115782223 11578222 3 Immunosuppressant drug therapy
115782223 11578222 4 Depression

Outcome of event

Event ID CASEID OUTC COD
115782223 11578222 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
115782223 11578222 Acute kidney injury
115782223 11578222 Decreased appetite
115782223 11578222 Dehydration
115782223 11578222 Diarrhoea
115782223 11578222 Weight decreased

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
115782223 11578222 1 20130525 0
115782223 11578222 3 20130530 0
115782223 11578222 4 20130708 0