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
126786421 12678642 1 I 20160812 20160815 20160823 20160823 EXP US-BAXALTA-2016BLT005965 BAXALTA 66.85 YR F Y 0.00000 20160823 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
126786421 12678642 1 PS GAMMAGARD LIQUID HUMAN IMMUNOGLOBULIN G 1 Subcutaneous 8 G, 1X A WEEK LE12R056AB 125105 8 G SOLUTION FOR INFUSION /wk
126786421 12678642 2 SS GAMMAGARD LIQUID HUMAN IMMUNOGLOBULIN G 1 Subcutaneous UNK LE12R090AC 125105 SOLUTION FOR INFUSION
126786421 12678642 3 SS GAMMAGARD LIQUID HUMAN IMMUNOGLOBULIN G 1 Subcutaneous 8 G, 1X A WEEK IN THE ABDOMEN 125105 8 G SOLUTION FOR INFUSION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126786421 12678642 1 Immunodeficiency common variable

Outcome of event

Event ID CASEID OUTC COD
126786421 12678642 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126786421 12678642 Blood glucose decreased
126786421 12678642 Infusion site erythema
126786421 12678642 Infusion site pain
126786421 12678642 Infusion site swelling
126786421 12678642 Injection site pruritus
126786421 12678642 Unresponsive to stimuli

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
126786421 12678642 1 20160812 0
126786421 12678642 2 20160812 0
126786421 12678642 3 20160805 0