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
126965331 12696533 1 I 20130312 20120316 20160830 20160830 EXP US-ROCHE-1354605 ROCHE 69.13 YR F Y 0.00000 20160830 MD 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
126965331 12696533 1 PS ROCEPHIN CEFTRIAXONE SODIUM 1 Unknown 63239
126965331 12696533 2 SS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Oral 50723 500 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126965331 12696533 1 Product used for unknown indication
126965331 12696533 2 Lung transplant

Outcome of event

Event ID CASEID OUTC COD
126965331 12696533 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126965331 12696533 Death
126965331 12696533 Hypersensitivity

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

no results found

Therapies reported

no results found