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
123518113 12351811 3 F 201601 20160803 20160510 20160815 EXP US-BAXALTA-2016BLT003085 BAXALTA 78.02 YR M Y 0.00000 20160815 OT 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
123518113 12351811 1 PS GAMMAGARD LIQUID HUMAN IMMUNOGLOBULIN G 1 Intravenous (not otherwise specified) 45 G, 1X A MONTH 125105 45 G SOLUTION FOR INFUSION /month
123518113 12351811 2 SS GAMMAGARD LIQUID HUMAN IMMUNOGLOBULIN G 1 Intravenous (not otherwise specified) 45 G, 1X A MONTH 125105 45 G SOLUTION FOR INFUSION /month
123518113 12351811 3 SS VICTOZA LIRAGLUTIDE 1 Unknown UNK N 0
123518113 12351811 4 C PREDNISONE. PREDNISONE 1 Unknown 60 MG, 1X A DAY U 0 60 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123518113 12351811 1 Immunodeficiency common variable
123518113 12351811 3 Diabetes mellitus
123518113 12351811 4 Visual impairment

Outcome of event

Event ID CASEID OUTC COD
123518113 12351811 OT
123518113 12351811 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123518113 12351811 Atrial fibrillation
123518113 12351811 Functional gastrointestinal disorder
123518113 12351811 Kidney infection
123518113 12351811 Nausea
123518113 12351811 Renal failure
123518113 12351811 Sepsis
123518113 12351811 Urinary tract infection

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
123518113 12351811 1 201310 0
123518113 12351811 2 20160701 0