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
126515351 12651535 1 I 201603 20160801 20160815 20160815 EXP GB-VELOXIS PHARMACEUTICALS-1056311 VELOXIS PHARMACEUTICALS 60.00 YR F Y 0.00000 20160815 MD GB GB

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
126515351 12651535 1 PS ENVARSUS XR TACROLIMUS 1 Unknown U 206406 PROLONGED-RELEASE TABLET
126515351 12651535 2 SS PREDNISONE. PREDNISONE 1 U 0
126515351 12651535 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 0 500 MG QOW
126515351 12651535 4 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 0 1200 MG QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126515351 12651535 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126515351 12651535 OT
126515351 12651535 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126515351 12651535 Drug ineffective
126515351 12651535 Herpes zoster
126515351 12651535 Incorrect dose administered
126515351 12651535 Metapneumovirus infection
126515351 12651535 Osteonecrosis
126515351 12651535 Respiratory tract infection

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

no results found

Therapies reported

no results found